Combination therapies comprising quinoxaline inhibitors of p13k-alpha for use in the treatment of cancer

ABSTRACT

The present invention provides methods of treating cancer by administering a compound of Formula I, optionally as a pharmaceutically acceptable salt, solvate and/or hydrate thereof, in combination with other cancer treatments.

CROSS-REFERENCE TO RELATED APPLICATIONS

The Applicants claim priority under 35 U.S.C. 119(e) to copending Provisional Application No. 60/923,164 filed on Apr. 11, 2007, the disclosure of which is incorporated herein by reference in its entirety.

FIELD OF THE INVENTION

This invention relates to methods of treating cancer with a compound that inhibits lipid kinase enzymatic activity and the resultant modulation of cellular activities (such as proliferation, differentiation, programmed cell death, migration, chemoinvasion and metabolism) in combination with anticancer agents.

BACKGROUND OF THE INVENTION

Improvements in the specificity of agents used to treat various disease states such as cancer, metabolic, and inflammatory diseases is of considerable interest because of the therapeutic benefits which would be realized if the side effects associated with the administration of these agents could be reduced. Traditionally, dramatic improvements in the treatment of cancer are associated with identification of therapeutic agents acting through novel mechanisms.

Phosphatidylinositol 3-kinase (PI3K or PIK3CA) is composed of an 85 kDa regulatory subunit and a 110 kDa catalytic subunit. The protein encoded by this gene represents the catalytic subunit, which uses ATP to phosphorylate PtdIns, PtdIns4P and PtdIns(4,5)P2. PTEN, a tumor suppressor which inhibits cell growth through multiple mechanisms, can dephosphorylate PIP3, the major product of PIK3CA. PIP3, in turn, is required for translocation of protein kinase B (AKT1, PKB) to the cell membrane, where it is phosphorylated and activated by upstream kinases. The effect of PTEN on cell death is mediated through the PIK3CA/AKT1 pathway.

PI3Kα has been implicated in the control of cytoskeletal reorganization, apoptosis, vesicular trafficking, proliferation and differentiation processes. Increased copy number and expression of PIK3CA or activating mutations in the p110a catalytic subunit of PIK3CA are associated with a number of malignancies such as ovarian cancer (Campbell et al., Cancer Res 2004, 64, 7678-7681; Levine et al., Clin Cancer Res 2005, 11, 2875-2878; Wang et al., Hum Mutat 2005, 25, 322; Lee et al., Gynecol Oncol 2005, 97, 26-34), cervical cancer, breast cancer (Bachman, et al. Cancer Biol Ther 2004, 3, 772-775; Levine, et al., supra; Li et al., Breast Cancer Res Treat 2006, 96, 91-95; Saal et al., Cancer Res 2005, 65, 2554-2559; Samuels and Velculescu, Cell Cycle 2004, 3, 1221-1224), colorectal cancer (Samuels, et al. Science 2004, 304, 554; Velho et al. Eur J Cancer 2005, 41, 1649-1654), endometrial cancer (Oda et al. Cancer Res. 2005, 65, 10669-10673), gastric carcinomas (Byun et al., Int J Cancer 2003, 104, 318-327; Li et al., supra; Velho et al., supra; Lee et al., Oncogene 2005, 24, 1477-1480), hepatocellular carcinoma (Lee et al., id.), small and non-small cell lung cancer (Tang et al., Lung Cancer 2006, 51, 181-191; Massion et al., Am J Respir Crit. Care Med 2004, 170, 1088-1094), thyroid carcinoma (Wu et al., J Clin Endocrinol Metab 2005, 90, 4688-4693), acute myelogenous leukemia (AML) (Sujobert et al., Blood 1997, 106, 1063-1066), chronic myelogenous leukemia (CML) (Hickey and Cotter J Biol Chem 2006, 281, 2441-2450), and glioblastomas (Hartmann et al. Acta Neuropathol (Berl) 2005, 109, 639-642; Samuels et al., supra).

In view of the important role of PI3K-α in biological processes and disease states, inhibitors and/or modulators of this lipid kinase are desirable. In addition, it is well established that combining treatments with different mechanisms of action often leads to enhanced anti-tumor activity as compared to single treatments administered alone. This is true for combinations of chemotherapies (e.g. Kyrgiou M. et. al. J Natl Cancer Inst 2006, 98, 1655) and combinations of antibodies and chemotherapy (e.g. Pasetto L M et. al. Anticancer Res 2006, 26, 3973.

For example, activation of the PI3K pathway contributes to the resistance of human tumor cells to a wide variety of chemotherapeutic agents, including microtubule stabilizing agents such as taxol (Brognard, J., et. al. Cancer Res 2001, 61, 3986-3997; Clark, A. S., et. al. Mol Cancer Ther 2002, 1, 707-717; Kraus, A. C., et. al. Oncogene 2002, 21, 8683-8695; Krystal, G. W., et. al. Mol Cancer Ther 2002, 1, 913-922; and Yuan, Z. Q., et. al. J Biol Chem 2003, 278, 23432-23440). Taxol is widely used to treat advanced cancers including prostate carcinomas, which frequently harbor deletions in the PTEN gene, resulting in elevated signaling downstream of PI3K. A number of preclinical studies suggest that inhibiting signaling downstream of PI3K restores or enhances the ability of chemotherapeutic agents such as taxol to kill tumor cells (Brognard, J., et. al. Cancer Res 2001, 61, 3986-3997; Clark, A. S., et. al. Mol Cancer Ther 2002, 1, 707-717; Kraus, A. C., et. al. Oncogene 2002, 21, 8683-8695; Krystal, G. W., et. al. Mol Cancer Ther 2002, 1, 913-922; and Saga, Y., et. al. Clin Cancer Res 2002, 8, 1248-1252).

Rapamycin, another chemotherapeutic agent, is a potent inhibitor of the mTOR/Raptor complex. Inhibition of mTOR/Raptor prevents p70S6K and S6 phosphorylation, but also leads to relief of a negative feedback loop emanating from p70S6K that serves to downregulate PI3K (Sarbassov, D. D., et. al. Science 2005, 307, 1098-1101). As a result, rapamycin treatment can lead to upregulation of PI3K and increased phosphorylation of AKT (O'Donnell, A., et. al. paper presented at Proc Am Soc Clin Oncol. 2003; and O'Reilly, K. E., et. al. Cancer Res 2006, 66, 1500-1508). Thus, combining rapamycin with inhibitors of PI3K can enhance the efficacy of rapamycin (Powis, G. et. al. Clinical Cancer Research 2006, 12, 2964-2966; Sun, S.-Y., et. al. Cancer Research 2005, 65, 7052-7058).

A growing body of clinical and preclinical data indicates that activation of the PI3K pathway confers resistance to EGFR inhibitors such as erlotinib (Bianco, R., et. al. Oncogene 2003, 22, 2812-2822; Chakravarti, A., et. al. Cancer Res 2002, 62, 200-207; and Janmaat, M. L., et. al. Clin Cancer Res 2003, 9, 2316-2326). Both NSCLC patients with K-Ras mutations and glioblastoma patients with PTEN deletions fail to respond to erlotinib, potentially because of genetic activation of the PI3K pathway (Mellinghoff, I. K., et. al. N. Eng. J Med. 2006, 353, 2012-2024). Preclinical studies have shown that downregulation of PI3K signaling in EGFR-expressing tumor cells confers increased sensitivity to EGFR inhibitors (Ihle, N. T., et. al. Mol Cancer Ther 2005, 4, 1349-1357). Thus, treating cancer with a PI3K inhibitor in combination with an EGFR inhibitor, such as erlotinib, is desirable.

Activation of the PI3K pathway also contributes to the resistance of human tumor cells to DNA damaging agents, such as platins. A number of preclinical studies suggest that inhibiting signaling downstream of PI3K restores or enhances the ability of chemotherapeutic agents such as platins to kill tumor cells (Brognard, J., et. al. Cancer Res 2001, 61, 3986-3997; and Yuan, Z. Q., et. al. J Biol Chem 2003, 278, 23432-23440). Carboplatin is widely used to treat advanced cancers including non-small cell lung carcinomas (NSCLC), which frequently harbor activating mutations in the K-Ras gene, resulting in activation of PI3K (Aviel-Ronen S., et. al. Clin Lung Cancer 2006, 8, 30-38). NSCLC patients with K-Ras mutations do not respond to EGFR inhibitors such as Tarceva, and thus represent a significant unmet medical need (Janne P A, et. al. J Clin Oncology 2005, 23, 3227-3234). Thus, treating NSCLC with a DNA-damaging agent such as a platin in combination with an inhibitor of PI3K is desirable in light of the lack of efficacious treatments.

Treatments that combine an inhibitor of PI3K-α with other anti-cancer agents are desirable and needed.

SUMMARY OF THE INVENTION

The following only summarizes certain aspects of the invention and is not intended to be limiting in nature. These aspects and other aspects and embodiments are described more fully below. All references cited in this specification are hereby incorporated by reference in their entirety. In the event of a discrepancy between the express disclosure of this specification and the references incorporated by reference, the express disclosure of this specification shall control.

The compositions of the invention are used to treat diseases associated with abnormal and or unregulated cellular activities. Disease states which can be treated by the methods and compositions provided herein include cancer. The invention is directed to methods of treating these diseases by administering a Compound of Formula I or II in combination with one or more treatments.

One aspect of the Invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a compound of Formula I:

or a single isomer thereof where the compound is optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof; or administering a pharmaceutical composition comprising a therapeutically effective amount of a compound of Formula I and a pharmaceutically acceptable carrier, excipient, or diluent in combination with one or more treatments independently selected from surgery, one or more chemotherapeutic agents, one or more hormone therapies, one or more antibodies, one or more immunotherapies, radioactive iodine therapy, and radiation, where the Compound of Formula I is that wherein:

-   W¹, W², W³, and W⁴ are —C(R¹)═; or one or two of W¹, W², W³, and W⁴     are independently —N═ and the remaining are —C(R¹)═; and where each     R¹ is independently hydrogen, alkyl, haloalkyl, nitro, alkoxy,     haloalkoxy, halo, hydroxy, cyano, amino, alkylamino, or     dialkylamino; -   R⁵¹ is hydrogen or alkyl; -   R⁵² is hydrogen or halo; -   R⁵⁰, R⁵³, and R⁵⁴ are independently hydrogen, alkyl, alkenyl, halo,     haloalkyl, haloalkenyl, hydroxy, alkoxy, alkenyloxy, haloalkoxy,     nitro, amino, alkylamino, dialkylamino,     —N(R⁵⁵)C(O)—C₁-C₆-alkylene-N(R^(55a))R^(55b), alkylcarbonyl,     alkenylcarbonyl, carboxy, alkoxycarbonyl, cyano, alkylthio,     —S(O)₂NR⁵⁵R^(55a), or alkylcarbonylamino and where R⁵⁵ and R^(55b)     are independently hydrogen, alkyl, or alkenyl and R^(55a) is     hydrogen, alkyl, alkenyl, hydroxy, or alkoxy; or R⁵³ and R⁵⁴     together with the carbons to which they are attached form a 5- or     6-membered heteroaryl or 5- or 6-membered heterocycloalkyl; -   B is phenyl substituted with R^(3a) and optionally further     substituted with one, two, or three R³; or -   B is heteroaryl optionally substituted with one, two, or three R³; -   R^(3a) is cyano; hydroxyamino; carboxy; alkoxycarbonyl; alkylamino;     dialkylamino; alkylcarbonyl; haloalkoxy; alkylsulfonyl;     aminoalkyloxy; alkylaminoalkyloxy; dialkylaminoalkyloxy; or     -   a) —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)) where R⁷ is         hydrogen, alkyl, or alkenyl and R^(7a) and R^(7b) are         independently hydrogen, alkyl, alkenyl, hydroxyalkyl, haloalkyl,         alkoxy, alkoxyalkyl, aminoalkyl, alkylaminoalkyl,         dialkylaminoalkyl, cycloalkyl, cycloalkylalkyl,         heterocycloalkyl, heterocycloalkylalkyl, heteroaryl,         heteroarylalkyl, aryl, arylalkyl, or arylalkyloxy and where the         aryl, cycloalkyl, heterocycloalkyl and heteroaryl rings in         R^(7a) and R^(7b) (either alone or as part of arylalkyl,         cycloalkylalkyl, heterocycloalkylalkyl and heteroarylalkyl) are         independently optionally substituted with 1, 2, or 3 groups         independently selected from alkyl, amino, alkylamino,         dialkylamino, hydroxy, halo, alkoxy, alkylthio, and oxo);     -   b) —C(O)NR⁸R^(8a) where R⁸ is hydrogen, hydroxy, alkoxy, alkyl,         alkenyl, haloalkyl, or haloalkoxy and R^(8a) is hydrogen, alkyl,         alkenyl, hydroxyalkyl, cyanoalkyl, alkoxyalkyl, alkylthioalkyl,         heterocycloalkyl, heterocycloalkylalkyl, cycloalkyl,         cycloalkylalkyl, heteroaryl, heteroarylalkyl, aryl, or arylalkyl         and where the aryl, cycloalkyl, heteroaryl, and heterocycloalkyl         rings in R^(8a) (either alone or as part of arylalkyl,         cycloalkylalkyl, heterocycloalkylalkyl and heteroarylalkyl) are         independently optionally substituted with 1, 2, or 3 groups         independently selected from alkyl, alkenyl, alkoxy, halo,         haloalkyl, haloalkoxy, hydroxy, hydroxyalkyl, oxo, amino,         alkylamino, dialkylamino, alkylcarbonyl, aminoalkyl,         alkylaminoalkyl, dialkylaminoalkyl, alkoxycarbonyl, and —C(O)H;     -   c) —NR⁹C(O)R^(9a) where R⁹ is hydrogen, hydroxy, alkoxy, alkyl,         alkenyl, haloalkyl, or haloalkoxy and R^(9a) is hydrogen,         C₂-C₆-alkyl, alkenyl, hydroxyalkyl, alkoxyalkyl, cycloalkyl,         cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl,         heteroaryl, heteroarylalkyl, aryl, or arylalkyl; where the aryl,         cycloalkyl, heteroaryl, and heterocycloalkyl rings in R^(9a)         (either alone or as part of arylalkyl, cycloalkylalkyl,         heterocycloalkylalkyl and heteroarylalkyl) are independently         optionally substituted with 1, 2, or 3 groups independently         selected from alkyl, alkenyl, alkoxy, hydroxy, hydroxyalkyl,         halo, haloalkyl, haloalkoxy, oxo, amino, alkylamino,         dialkylamino, alkylcarbonyl, alkoxycarbonyl, —C(O)H, aryl         (optionally substituted with one or two halo), arylalkyl,         heteroaryl, heteroarylalkyl, heterocycloalkyl,         heterocycloalkylalkyl, cyloalkyl, cyloalkylalkyl, and         cycloalkylcarbonyl;     -   d) —C(O)N(R¹⁰)—C₁-C₆-alkylene-N(R^(10a))R^(10b) where R^(10a) is         hydrogen, hydroxy, alkoxy, alkyl, alkenyl, haloalkyl,         aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, or hydroxyalkyl         and R¹⁰ and R^(10b) are independently hydrogen, alkyl, alkenyl,         haloalkyl, aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, or         hydroxyalkyl;     -   e) —NR¹¹C(O)NR^(11a)R^(11b) where R^(11a) is hydrogen, alkyl,         alkenyl, hydroxy, or alkoxy and R¹¹ and R^(11b) are         independently hydrogen, alkyl, alkenyl, aminoalkyl,         alkylaminoalkyl, or dialkylaminoalkyl;     -   f) —C(O)R¹² where R¹² is heterocycloalkyl optionally substituted         with 1, 2, or 3 groups selected from alkyl, oxo, amino,         alkylamino, and heterocycloalkylalkyl;     -   g) —NR¹³C(O)OR^(13a) where R¹³ is hydrogen, alkyl, or alkenyl         and R^(13a) is aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl,         aryl, or arylalkyl;     -   h) —C(O)N(R¹⁴)N(R^(14a))(R^(14b)) where R¹⁴, R^(14a), and         R^(14b) are independently hydrogen, alkyl, or alkenyl;     -   i) —S(O)₂N(R¹⁵)—C₁-C₆-alkylene-N(R^(15a))R^(15b) where R¹⁵,         R^(15a), and R^(15b) are independently hydrogen, alkyl, or         alkenyl;     -   j) —C(O)N(R¹⁶)—C₁-C₆-alkylene-C(O)OR^(16a) where R¹⁶ is         hydrogen, alkyl, or alkenyl and R^(16a) is alkyl or alkenyl;     -   k) heteroaryl optionally substituted with one or two aminoalkyl,         alkylaminoalkyl, or dialkylaminoalkyl;     -   l) —N(R¹⁷)—C(═N(R^(17b))(R^(17a)))(NR^(17c)R^(17d)) where R¹⁷,         R^(17a), R^(17b), R^(17c), and R^(17d) are independently         hydrogen, alkyl, or alkenyl;     -   m) —N(R¹⁸)C(O)—C₁-C₆-alkylene-N(R^(18b))C(O)R^(18a) where         R^(18a) is hydrogen, alkyl, alkenyl, or alkoxy and R¹⁸ and         R^(18b) are independently hydrogen, alkyl, or alkenyl;     -   n) —C(O)N(R¹⁹)—C₁-C₆-alkylene-C(O)R^(19a) where R¹⁹ is hydrogen,         alkyl, or alkenyl and R^(19a) is amino, alkylamino,         dialkylamino, or heterocycloalkyl;     -   o) —N(R²⁰)C(O)—C₁-C₆-alkylene-C(O)R^(20a) where R²⁰ is hydrogen,         alkyl, or alkenyl and R^(20a) is cycloalkyl or heterocycloalkyl;     -   p) —NR²¹S(O)₂—C₁-C₆-alkylene-N(R^(21b))R^(21a) where R²¹ is         hydrogen, alkyl, or alkenyl and R^(21a) and R^(21b) are         independently hydrogen, alkyl, or alkenyl;     -   q) —N(R²²)C(O)—C₁-C₆-alkylene-N(R^(22b))—N(R^(22c))(R^(22a))         where R²², R^(22a) and R^(22b) are independently hydrogen,         alkyl, or alkenyl;     -   r) —C₀₋C₆-alkylene-N(R²³)—C₁-C₆-alkylene-N(R^(23b))R^(23a) where         R²³, R^(23a) and R^(23b) are independently hydrogen, alkyl, or         alkenyl; or     -   s) —NR²⁴C(O)—C₁₋C₆-alkylene-OR^(24a) where R²⁴ is hydrogen,         alkyl, or alkenyl and R^(24a) is alkoxyalkyl or aryl optionally         substituted with one or two halo or alkyl; and -   where each of the alkylene in R^(3a) is independently optionally     further substituted with 1, 2, 3, 4, or 5 groups selected from halo,     hydroxy, amino, alkylamino, and dialkylamino; and -   each R³ (when R³ is present) is independently alkyl; alkenyl;     alkynyl; halo; hydroxy; oxo; alkoxy; cyano; hydroxyamino; carboxy;     alkoxycarbonyl; amino; alkylamino; dialkylamino; alkylcarbonyl;     haloalkoxy; alkylsulfonyl; aminoalkyloxy; alkylaminoalkyloxy;     dialkylaminoalkyloxy; or     -   a) —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)) where R⁷ is         hydrogen, alkyl, or alkenyl and R^(7a) and R^(7b) are         independently hydrogen, alkyl, alkenyl, hydroxyalkyl, haloalkyl,         alkoxy, alkoxyalkyl, aminoalkyl, alkylaminoalkyl,         dialkylaminoalkyl, cycloalkyl, cycloalkylalkyl,         heterocycloalkyl, heterocycloalkylalkyl, heteroaryl,         heteroarylalkyl, aryl, arylalkyl, or arylalkyloxy and where the         aryl, cycloalkyl, heterocycloalkyl and heteroaryl rings in         R^(7a) and R^(7b) (either alone or as part of arylalkyl,         cycloalkylalkyl, heterocycloalkylalkyl and heteroarylalkyl) are         independently optionally substituted with 1, 2, or 3 groups         independently selected from alkyl, amino, alkylamino,         dialkylamino, hydroxy, halo, alkoxy, alkylthio, and oxo);     -   b) —C(O)NR⁸R^(8a) where R⁸ is hydrogen, hydroxy, alkoxy, alkyl,         alkenyl, haloalkyl, or haloalkoxy and R^(8a) is hydrogen, alkyl,         alkenyl, hydroxyalkyl, cyanoalkyl, alkoxyalkyl, alkylthioalkyl,         heterocycloalkyl, heterocycloalkylalkyl, cycloalkyl,         cycloalkylalkyl, heteroaryl, heteroarylalkyl, aryl, or arylalkyl         and where the aryl, cycloalkyl, heteroaryl, and heterocycloalkyl         rings in R^(8a) (either alone or as part of arylalkyl,         cycloalkylalkyl, heterocycloalkylalkyl and heteroarylalkyl) are         independently optionally substituted with 1, 2, or 3 groups         independently selected from alkyl, alkenyl, alkoxy, halo,         haloalkyl, haloalkoxy, hydroxy, hydroxyalkyl, oxo, amino,         alkylamino, dialkylamino, alkylcarbonyl, aminoalkyl,         alkylaminoalkyl, dialkylaminoalkyl, alkoxycarbonyl, and —C(O)H;     -   c) —NR⁹C(O)R^(9a) where R⁹ is hydrogen, hydroxy, alkoxy, alkyl,         alkenyl, haloalkyl, or haloalkoxy and R^(9a) is hydrogen,         C₂-C₆-alkyl, alkenyl, hydroxyalkyl, alkoxyalkyl, cycloalkyl,         cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl,         heteroaryl, heteroarylalkyl, aryl, or arylalkyl; where the aryl,         cycloalkyl, heteroaryl, and heterocycloalkyl rings in R^(9a)         (either alone or as part of arylalkyl, cycloalkylalkyl,         heterocycloalkylalkyl and heteroarylalkyl) are independently         optionally substituted with 1, 2, or 3 groups independently         selected from alkyl, alkenyl, alkoxy, hydroxy, hydroxyalkyl,         halo, haloalkyl, haloalkoxy, oxo, amino, alkylamino,         dialkylamino, alkylcarbonyl, alkoxycarbonyl, —C(O)H, aryl         (optionally substituted with one or two halo), arylalkyl,         heteroaryl, heteroarylalkyl, heterocycloalkyl,         heterocycloalkylalkyl, cyloalkyl, cyloalkylalkyl, and         cycloalkylcarbonyl;     -   d) —C(O)N(R¹⁰)—C₁-C₆-alkylene-N(R^(10a))R^(10b) where R^(10a) is         hydrogen, hydroxy, alkoxy, alkyl, alkenyl, haloalkyl, or         hydroxyalkyl and R¹⁰ and R^(10b) are independently hydrogen,         alkyl, alkenyl, haloalkyl, or hydroxyalkyl;     -   e) —NR¹¹C(O)NR^(11a)R^(11b) where R^(11a) is hydrogen, alkyl,         alkenyl, hydroxy, or alkoxy and R¹¹ and R^(11b) are         independently hydrogen, alkyl, alkenyl, aminoalkyl,         alkylaminooalkyl, dialkylaminoalkyl;     -   f) —C(O)R¹² where R¹² is heterocycloalkyl optionally substituted         with 1, 2, or 3 groups selected from alkyl, oxo, amino,         alkylamino, and heterocycloalkylalkyl;     -   g) —NR¹³C(O)OR^(13a) where R¹³ is hydrogen, alkyl, or alkenyl         and R^(13a) is aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl,         aryl, or arylalkyl);     -   h) —C(O)N(R¹⁴)N(R^(14a))(R^(14b)) where R¹⁴, R^(14a), and         R^(14b) are independently hydrogen, alkyl, or alkenyl;     -   i) —S(O)₂N(R¹⁵)—C₁-C₆-alkylene-N(R^(15a))R^(15b) where R¹⁵,         R^(15a), and R^(15b) are independently hydrogen, alkyl, or         alkenyl;     -   j) —C(O)N(R¹⁶)—C₁-C₆-alkylene-C(O)OR^(16a) where R¹⁶ is         hydrogen, alkyl, or alkenyl and R^(16a) is alkyl or alkenyl;     -   k) heteroaryl optionally substituted with one or two aminoalkyl,         alkylaminoalkyl, or dialkylaminoalkyl;     -   l) —N(R¹⁷)—C(═N(R^(17b))(R^(17a)))(NR^(17c)R^(17d)) where R¹⁷,         R^(17a), R^(17b), R^(17c), and R^(17d) are independently         hydrogen, alkyl, or alkenyl;     -   m) —N(R¹⁸)C(O)—C₁-C₆-alkylene-N(R^(18b))C(O)R^(18a) where         R^(18a) is hydrogen, alkyl, alkenyl, or alkoxy and R¹⁸ and         R^(18b) are independently hydrogen, alkyl, or alkenyl;     -   n) —C(O)N(R¹⁹)—C₁-C₆-alkylene-C(O)R^(19a) where R¹⁹ is hydrogen,         alkyl, or alkenyl and R^(19a) is amino, alkylamino,         dialkylamino, or heterocycloalkyl;     -   o) —N(R²⁰)C(O)—C₁-C₆-alkylene-C(O)R^(20a) where R²⁰ is hydrogen,         alkyl, or alkenyl and R^(20a) is cycloalkyl or heterocycloalkyl;     -   p) —NR²¹S(O)₂—C₁-C₆-alkylene-N(R^(21b))R^(21a) where R²¹ is         hydrogen, alkyl, or alkenyl and R^(21a) and R^(21b) are         independently hydrogen, alkyl, or alkenyl;     -   q) —N(R²²)C(O)—C₁-C₆-alkylene-N(R^(22b))—N(R^(22c))(R^(22a)),         where R²², R^(22a) and R^(22b) are independently hydrogen,         alkyl, or alkenyl;     -   r) —C₀₋C₆-alkylene-N(R²³)—C₁-C₆-alkylene-N(R^(23b))R^(23a) where         R²³, R^(23a) and R^(23b) are independently hydrogen, alkyl, or         alkenyl; or     -   s) —NR²⁴C(O)—C₁₋C₆-alkylene-OR^(24a) where R²⁴ is hydrogen,         alkyl, or alkenyl and R^(24a) is alkoxyalkyl or aryl optionally         substituted with one or two halo or alkyl; -   wherein each of the alkylene in R³ is independently optionally     further substituted with 1, 2, 3, 4, or 5 groups selected from halo,     hydroxy, amino, alkylamino, and dialkylamino; and -   provided that when R⁵⁰ and R⁵² are hydrogen, R⁵¹ is hydrogen or     methyl, R⁵³ is hydrogen or methoxy, and R⁵⁴ is hydrogen or methoxy,     then B is not 2,3-dihydro-1,4-benzodioxinyl, thien-2-yl, or     thien-2-yl substituted with one R³ where R³ is halo.

A second aspect of the Invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a compound of Formula II:

or a pharmaceutically acceptable salt or solvate, thereof; or administering a pharmaceutical composition comprising a therapeutically effective amount of a compound of Formula II and a pharmaceutically acceptable carrier, excipient, or diluent in combination with one or more treatments independently selected from surgery, one or more chemotherapeutic agents, one or more of the hormone therapies, one or more of the antibodies, one or more immunotherapies, radioactive iodine therapy, and radiation wherein the Compound of Formula I is that wherein:

-   W¹, W², W³, and W⁴ are —C(R^(1a))═; or one or two of W¹, W², W³, and     W⁴ are independently —N═ and the remaining are —C(R^(1a))═; -   X′ is —N(R^(5a))—; -   A is aryl, —S(O)₂-aryl, heteroaryl, cycloalkyl, heterocycloalkyl,     halo, haloalkyl, haloalkoxy, alkyl, alkoxy, or -alkyl-N(R⁷)R^(7a),     where each of the aryl, heteroaryl, cycloalkyl, heterocycloalkyl,     alkyl and alkoxy groups, each either alone or as part of another     group within A, are independently optionally substituted with one,     two, three, or four R^(2a); or -   B¹ is aryl, arylalkyl, alkyl, heteroaryl, or heteroaryalkyl, wherein     each of the aryl, heteroaryl and alkyl groups are independently     optionally substituted with one, two, three, or four R^(3d); -   each R^(1a) is independently selected from hydrogen, alkoxy, alkyl,     nitro, halo, cyano, and —C₀-C₆-alkyl-N(R⁷)R^(7a), wherein each of     the alkyl and alkoxy groups is optionally substituted with 1, 2, 3,     4, or 5 groups selected from alkyl, alkoxy, halo, haloalkyl,     haloalkoxy, nitro, cyano, hydroxy, —N(R⁸)R^(8a), and —C(O)OR⁶; -   each R^(2a) (when R^(2a) is present) is independently selected from     alkyl, alkenyl, -alkenyl-C(O)OR⁶, —OR⁶, —N(R⁷)C(O)R⁶,     —N(R⁷)C(O)—C₀-C₆ alkyl-N(R^(7b))R^(7a), —OC(O)—C₀-C₆     alkyl-N(R⁷)R^(7a), —N(R⁷)C(O)—C₁-C₆ alkylC(O)OR⁶,     C₀-C₆-alkyl-C(O)R⁶, oxo, dioxo, —S(O)₂—N(R⁷)R^(7a), —C(O)OR⁶,     —CH(R⁶)₂—C(O)OR⁶, —S(O)₂R⁶, cycloalkyl, heterocycloalkyl,     heteroaryl, —C(O)N(R⁷)-alkyl-OR⁶, —C₀-C₆     alkyl-C(O)N(R⁷)—C₀-C₆-alkyl-C(O)OR⁶, —C₀-C₆-alkyl-C(O)N(R⁷)R^(7a),     aryl, arylalkyl, —S—(C₁-C₆ alkyl), halo, oxo, nitro, —SCN, cyano,     and —C₀-C₆ alkyl-N(R⁷)R^(7a), wherein each of the alkyl (including,     for example the alkyl within alkoxy), aryl, cycloalkyl,     heterocycloalkyl, and heteroaryl groups, either alone or as part of     another group within R², is independently optionally substituted     with 1, 2, 3, 4, or 5 groups selected from alkyl, halo, haloalkyl,     haloalkoxy, oxo, nitro, cyano, hydroxy, —N(R⁸)R^(8a), alkoxy, and     —C(O)OR⁹; -   each R^(3d) (when R^(3d) is present) is independently oxo, nitro,     halo, cyano, alkyl, alkenyl, alkynyl, alkoxy, C₃-C₆-cycloalkyl,     —C₀-C₆-alkyl-heterocycloalkyl, —C₀-C₆     alkyl-N(R⁷)C(O)—C₀-C₆-alkyl-N(R^(7b))R^(7a), —C₀-C₆     alkyl-N(R⁷)C(O)—C₀-C₆-alkyl-N(R^(7b))C(O)R^(7a), —C₀-C₆     alkyl-C(O)—C₀-C₆-alkyl-N(R⁷)R^(7a),     —C₀-C₆-alkyl-C(O)N(R⁷)—C₀-C₆-alkyl-N(R^(7b))R^(7a),     —C₀-C₆-alkyl-C(O)N(R⁷)—C₁-C₆alkylC(O)OR^(7a), —C₀-C₆     alkyl-N(R⁷)C(O)—C₀-C₆-alkyl-(R^(7a)), —C₀-C₆     alkyl-N(R⁷)—C₀-C₆-alkyl-N(R^(7b))R^(7a), —C₀-C₆     alkyl-N(R⁷)C(O)—C₀-C₆-alkyl-N(R^(7b))—N(R^(7c))R^(7a), —C₀-C₆     alkyl-N(R⁷)C(O)O—C₀-C₆-alkyl-aryl, —C₀-C₆     alkyl-C(O)N(R⁷)—C₀-C₆-alkyl-N(R^(7b))R^(7a), —C₀-C₆     alkyl-N(R⁷)—C₀-C₆ alkyl-C(═N(R^(7b))(R^(7a)))(NR^(7c)R^(7d)),     —C₀-C₆-alkyl-aryl, —C₀-C₆-alkyl-heteroaryl, —C₀-C₆     alkyl-heterocycloalkyl, —O—C₀₋C₆ alkyl-N(R⁷)R^(7a), —C₀-C₆     alkyl-OR₆, —C₀-C₆ alkyl-C(O)OR₆, C₀-C₆-alkyl-N(R⁷)R^(7a), —C₀-C₆     alkyl-C(O)NR₇R^(7a), —C₀-C₆ alkyl-C(O)R⁷, —SR_(S), —S(O)₂R₇,     —S(O)₃R₇, —S(O)R⁷, —SO₂N(R⁷)R^(7a),     —SO₂N(R⁷)—C₀-C₆-alkyl-N(R^(7b))R^(7a), —C₀-C₆-alkyl-N(R⁷)-aryl,     —C₀-C₆-alkyl-N(R⁷)-heteroaryl, —C₀-C₆-alkyl-N(R⁷)— heterocycloalkyl,     —C₀-C₆-alkyl-C(O)N(R⁷)—C₀-C₆-alkyl-cycloalkyl,     C₀-C₆-alkyl-C(O)N(R⁷)—C₀-C₆-alkyl-aryl, C₀-C₆ alkyl-C(O)N(R⁷)—C₀-C₆     alkyl-heteroaryl,     C₀-C₆-alkyl-C(O)N(R⁷)—C₀-C₆-alkyl-heterocycloalkyl,     —C₀-C₆-alkyl-N(R⁷)C(O)—C₀-C₆-alkyl-cycloalkyl,     —C₀-C₆-alkyl-N(R⁷)C(O)—C₀-C₆-alkyl-aryl,     C₀-C₆-alkyl-N(R⁷)C(O)—C₀-C₆-alkyl-heteroaryl,     —C₀-C₆-alkyl-N(R⁷)C(O)—C₀-C₆-alkyl-heterocycloalkyl,     C₀-C₆-alkyl-N(R⁷)C(O)—C₀-C₆-alkyl-heterocycloalkyl-aryl,     —N(R⁷)C(O)OR⁶, or —NHC(O)H, wherein each of the alkyl, alkenyl,     cycloalkyl, aryl, (including, for example the alkyl within alkoxy),     heterocycloalkyl, and heteroaryl groups, either alone or as part of     another group within R^(3d), is independently optionally substituted     with 1, 2, 3, 4, or 5 groups selected from alkyl, alkenyl,     cycloalkyl, halo, haloalkyl, haloalkoxy, —C(O)R⁹, nitro, cyano, oxo,     —C₀-C₆-alkyl-N(R⁸)R^(8a), cycloalkyl, cycloalkylalkyl,     heterocycloalkyl, heterocycloalkylalkyl, aryl, arylalkyl,     heteroaryl, heteroarylalkyl, —C(O)OR⁹, alkylthio, and hydroxyalkyl; -   R⁴ is hydrogen, aryl, —C₀-C₆-alkyl-N(R⁷)R^(7a), alkoxy, or C₁-C₆     alkyl, wherein each of the alkyl and aryl groups, either alone or as     part of another group in R⁴, is independently optionally substituted     with 1, 2, 3, 4, or 5 groups selected from alkyl, halo, haloalkyl,     haloalkoxy, nitro, cyano, hydroxy, —N(R⁸)R^(8a), alkoxy, and     —C(O)OR⁶; or -   R⁴ and X¹ together with the atoms to which they are attached form a     heterocycloalkyl or heteroaryl group, wherein R^(5a) is absent when     X is —N(R^(5a))—, wherein each of the heterocycloalkyl or heteroaryl     is optionally substituted with 1, 2, 3, 4, or 5 groups selected from     alkyl, halo, haloalkyl, haloalkoxy, nitro, cyano, hydroxy,     —N(R⁷)R^(7a), alkoxy, and —C(O)OR⁶; -   R^(5a) is hydrogen, —C₁-C₆ alkyl-N(R⁷)R^(7a), alkoxy, alkyl, or     aryl, wherein each of the alkyl and aryl is optionally substituted     with 1, 2, 3, 4, or 5 groups selected from alkyl, halo, haloalkyl,     haloalkoxy, nitro, cyano, hydroxy, —N(R⁸)R^(8a), C₁-C₆ alkoxy, or     —C(O)OR⁶; or -   R^(5a) and R⁴ together with the atoms to which they are attached     form a heterocycloalkyl or heteroaryl group, wherein the     heterocycloalkyl and heteroaryl is optionally substituted with 1, 2,     3, 4, or 5 groups selected from alkyl, halo, haloalkyl, haloalkoxy,     nitro, cyano, hydroxy, —N(R⁷)R^(7a), C₁-C₆ alkoxy, and —C(O)OR⁶; -   R⁶ and R⁹ are independently hydrogen, hydroxy, alkyl, aryl,     arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl,     heterocycloalkylalkyl, heteroaryl, heteroarylalkyl, or aryl, each     alkyl, aryl, cycloalkyl, heterocycloalkyl, and heteroaryl, either     alone or as part of another group within R⁶ and R⁹, is independently     optionally substituted with 1, 2, 3, 4, or 5 groups independently     selected from amino, hydroxy, alkoxy, alkyl, and halo; and -   R⁷, R^(7a) R^(7b), R^(7c), R^(7d), R⁸, and R^(8a) are independently     hydrogen, alkyl, alkenyl, hydroxy, alkyloxy, alkenyloxy, —O—C₀-C₆     alkyl-aryl, —C₀-C₆ alkyl-C(O)OR⁶, —C₀-C₆ alkyl-C(O)R⁶, aryl,     arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl, cycloalkylalkyl,     heterocycloalkyl, or heterocycloalkylalkyl, wherein each of the     alkyl, aryl, heteroaryl, and heterocycloalkyl, either alone or part     of another group within R⁷, R^(7a) R^(7b), R^(7c), R^(7d), R⁸, and     R^(8a) is independently optionally substituted with 1, 2, 3, 4, or 5     groups selected from amino, alkylamino, dialkylamino, aminoalkyl,     alkylaminoalkyl, dialkylaminoalkyl, —S—C₁-C₆ alkyl, cyano, nitro,     hydroxy, C₁-C₆ alkoxy, C₁-C₆ alkyl, halo, aryl,     heterocycloalkylalkyl, and heteroaryl optionally substituted with     one or two C₁-C₆ alkyl.

DETAILED DESCRIPTION OF THE INVENTION Abbreviations and Definitions

The following abbreviations and terms have the indicated meanings throughout:

Abbreviation Meaning br broad ° C. degrees Celsius CBZ CarboBenZoxy = benzyloxycarbonyl d doublet dd doublet of doublet dt doublet of triplet EI Electron Impact ionization Et Ethyl g gram(s) GC gas chromatography h or hr hour(s) HPLC high pressure liquid chromatography L liter(s) M molar or molarity m Multiplet mg milligram(s) MHz megahertz (frequency) Min minute(s) mL milliliter(s) mM Millimolar mmol millimole(s) mol mole(s) MS mass spectral analysis N normal or normality nM Nanomolar NMR nuclear magnetic resonance spectroscopy q Quartet RT Room temperature s Singlet s- Secondary t- Tertiary t or tr Triplet TFA trifluoroacetic acid THF Tetrahydrofuran μL microliter(s) μM Micromole(s) or micromolar

Definitions for a Compound of Formula I, Ia, and II

The symbol “—” means a single bond, “═” means a double bond, “≡” means a triple bond, and “

” means a single bond and optionally a double bond. When chemical structures are depicted or described, unless explicitly stated otherwise, all carbons are assumed to have hydrogen substitution to conform to a valence of four.

“Administration” and variants thereof (e.g., “administering” a compound) in reference to a compound of the invention means introducing the compound or a prodrug of the compound into the system of the animal in need of treatment. When a compound of the invention or prodrug thereof is provided in combination with one or more other active agents (e.g., surgery, radiation, and chemotherapy, etc.), “administration” and its variants are each understood to include concurrent and sequential introduction of the compound or prodrug thereof and other agents.

“Alkenyl” or “lower alkenyl” means a straight or branched hydrocarbon radical having from 2 to 6 carbon atoms and at least one double bond and includes ethenyl, propenyl, 1-but-3-enyl, 1-pent-3-enyl, 1-hex-5-enyl and the like.

“Alkenylcarbonyl” means a C(O)R group where R is alkenyl, as defined herein.

“Alkenyloxy” or “lower alkenyloxy” means an —OR group where R is alkenyl, as defined herein. Representative examples include methoxy, ethoxy, 1-methoxyprop-1-en-3-yl, propoxy, isopropoxy, cyclopropyloxy, cyclohexyloxy and the like.

“Alkoxy” or “lower alkoxy” means an —OR group where R is alkyl, as defined herein. Representative examples include methoxy, ethoxy, 1-methoxyprop-1-en-3-yl, propoxy, isopropoxy, cyclopropyloxy, cyclohexyloxy and the like.

“Alkoxyalkyl” means an alkyl group, as defined herein, substituted with one, two, or three alkoxy groups, as defined herein.

“Akoxycarbonyl” means a —C(O)OR group where R is alkyl as defined herein.

“Alkoxyycarbonylalkyl” means an alkyl group, as defined herein, substituted with one, two, or three alkoxycarbonyl groups, as defined herein.

“Alkyl” or “lower alkyl” means a linear or branched hydrocarbon group having one to six carbon atoms. Examples of lower alkyl groups include methyl, ethyl, propyl, isopropyl, butyl, s-butyl, t-butyl, isobutyl, pentyl, hexyl and the like. A “C₀” alkyl (as in “C₀-C₆-alkyl”) is a covalent bond. “C₆ alkyl” refers to, for example, n-hexyl, iso-hexyl, and the like.

“Alkylamino” means a —NHR radical where R is alkyl as defined herein, or an N-oxide derivative thereof, e.g., methylamino, ethylamino, n-, iso-propylamino, n-, iso-, tert-butylamino, or methylamino-N-oxide, and the like.

“Alkylaminoalkyl” means an alkyl group substituted with one or two alkylamino groups, as defined herein.

“Alkylaminoalkyloxy” means an —OR group where R is alkylaminoalkyl, as defined herein.

“Alkylcarbonyl” means a C(O)R group where R is alkyl, as defined herein.

“Alkylcarbonylamino” means a —NRC(O)R′ group where R is hydrogen or alkyl, as defined herein, and R′ is alkyl, as defined herein.

“Alkylene” refers to straight or branched divalent hydrocarbon, containing no unsaturation and having from two to eight carbon atoms. Examples of alkylene include eth-diyl (—CH₂CH₂—), prop-1,3-diyl (—CH₂CH₂CH₂—), 2,2-dimethylprop-1,3-diyl (—CH₂C(CH₃)₂CH₂—), and the like.

“Alkylsulfonyl” means a —S(O)₂R group where R is alkyl, as defined herein.

“Alkylthio” means a —SR group where R is alkyl, as defined herein. Examples of alkylthio include methylthio and ethylthio, and the like.

“Alkylthioalkyl” means an alkyl group substituted with one or two alkylthio groups, as defined herein, e.g. 2-(methylthio)-ethyl and 2-(ethylthio)-ethyl.

“Alkynyl” or “lower alkynyl” means a straight or branched hydrocarbon radical having from 2 to 6 carbon atoms and at least one triple bond and includes ethynyl, propynyl, butynyl, pentyn-2-yl and the like.

“Amino” means a —NH₂.

“Aminoalkyl” means an alkyl group substituted with at least one, for example one, two, or three, amino groups.

“Aminoalkyloxy” means an —OR group where R is aminoalkyl, as defined herein.

“Aryl” means a monovalent six- to fourteen-membered, mono- or bi-carbocyclic ring, wherein the monocyclic ring is aromatic and at least one of the rings in the bicyclic ring is aromatic. Representative examples include phenyl, naphthyl, and indanyl, and the like.

“Arylalkyl” means an alkyl group, as defined herein, substituted with one or two aryl groups, as defined herein. Examples include benzyl, phenethyl, phenylvinyl, phenylallyl and the like.

“Aryloxy” means a —OR group where R is aryl as defined herein.

“Arylalkyloxy” means a —OR group where R is arylalkyl as defined herein.

“Arylsulfonyl” means a —SO₂R group where R is aryl as defined herein.

“Carboxyalkyl” means an alkyl group, as defined herein, substituted with one, two, or three —C(O)OH groups.

“Carboxy ester” means a —C(O)OR group where R is lower alkyl, lower alkenyl, lower alkynyl, cycloalkyl, aryl or arylalkyl, each of which is defined herein. Representative examples include methoxycarbonyl, ethoxycarbonyl, and benzyloxycarbonyl, and the like.

“Cyanoalkyl” means an alkyl, alkenyl, or alkynyl radical, as defined herein, substituted with at least one, for example one, two, or three, cyano groups.

“Cycloalkyl” means a monocyclic or polycyclic hydrocarbon radical having three to thirteen carbon atoms. The cycloalkyl can be saturated or partially unsaturated, but cannot contain an aromatic ring. Cycloalkyl includes fused, bridged, and spiro ring systems. Examples of such radicals include cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl.

“Cycloalkylalkyl” means alkyl group substituted with one or two cycloalkyl groups, as defined herein. Representative examples include cyclopropylmethyl and 2-cyclobutyl-ethyl, and the like.

“Cycloalkylcarbonyl” means a —C(O)R group where R is cycloalkyl as defined herein.

“Dialkylamino” means a —NRR′ radical where R and R′ are independently alkyl as defined herein, or an N-oxide derivative, or a protected derivative thereof, e.g., dimethylamino, diethylamino, N,N-methylpropylamino or N,N-methylethylamino, and the like.

“Dialkylaminoalkyl” means an alkyl group substituted with one or dialkylamino groups, as defined herein.

“Dialkylaminoalkyloxy” means an —OR group where R is dialkylaminoalkyl, as defined herein.

“Fused ring system” and “fused ring” refer to a polycyclic ring system that contains bridged or fused rings; that is, where two rings have more than one shared atom in their ring structures. In this application, fused-polycyclics and fused ring systems are not necessarily all aromatic ring systems. Typically, but not necessarily, fused-polycyclics share a vicinal set of atoms, for example naphthalene or 1,2,3,4-tetrahydro-naphthalene. A spiro ring system is not a fused-polycyclic by this definition, but fused polycyclic ring systems of the invention may themselves have spiro rings attached thereto via a single ring atom of the fused-polycyclic. In some examples, as appreciated by one of ordinary skill in the art, two adjacent groups on an aromatic system may be fused together to form a ring structure. The fused ring structure may contain heteroatoms and may be optionally substituted with one or more groups. It should additionally be noted that saturated carbons of such fused groups (i.e. saturated ring structures) can contain two substitution groups.

“Haloalkoxy” means an —OR′ group where R′ is haloalkyl as defined herein, e.g., trifluoromethoxy or 2,2,2-trifluoroethoxy, and the like.

“Haloalkoxyalkyl” means an alkyl group, as defined herein, substituted with one, two, or three haloalkoxy, as defined herein.

“Halogen” or “halo” means fluoro, chloro, bromo and iodo.

“Haloalkenyl means an alkenyl group, as defined herein, substituted with one or more halogens, for example one to five halo atoms.

“Haloalkyl” means an alkyl group, as defined herein, substituted with one or more halogens, for example one to five halo atoms. Representative examples includes 2,2-difluoroethyl, trifluoromethyl, and 2-chloro-1-fluoroethyl, and the like.

“Heteroaryl” means a monocyclic, fused bicyclic, or fused tricyclic, monovalent radical of 5 to 14 ring atoms containing one or more, for example one, two, three, or four ring heteroatoms independently selected from —O—, (n is 0, 1, or 2), —N—, —N(R^(x))—, and the remaining ring atoms being carbon, wherein the ring comprising a monocyclic radical is aromatic and wherein at least one of the fused rings comprising a bicyclic or tricyclic radical is aromatic. One or two ring carbon atoms of any nonaromatic rings comprising a bicyclic or tricyclic radical may be replaced by a —C(O)—, —C(S)—, or —C(═NH)— group. R^(x) is hydrogen, alkyl, hydroxy, alkoxy, acyl, or alkylsulfonyl. Fused bicyclic radical includes bridged ring systems. Unless stated otherwise, the valency may be located on any atom of any ring of the heteroaryl group, valency rules permitting. In particular, when the point of valency is located on the nitrogen, R^(x) is absent. In another embodiment, the term heteroaryl includes, but is not limited to, 1,2,4-triazolyl, 1,3,5-triazolyl, phthalimidyl, pyridinyl, pyrrolyl, imidazolyl, thienyl, furanyl, indolyl, 2,3-dihydro-1H-indolyl (including, for example, 2,3-dihydro-1H-indol-2-yl or 2,3-dihydro-1H-indol-5-yl, and the like), isoindolyl, indolinyl, isoindolinyl, benzimidazolyl, benzodioxol-4-yl, benzofuranyl, cinnolinyl, indolizinyl, naphthyridin-3-yl, phthalazin-3-yl, phthalazin-4-yl, pteridinyl, purinyl, quinazolinyl, quinoxalinyl, tetrazoyl, pyrazolyl, pyrazinyl, pyrimidinyl, pyridazinyl, oxazolyl, isooxazolyl, oxadiazolyl, benzoxazolyl, quinolinyl, isoquinolinyl, tetrahydroisoquinolinyl (including, for example, tetrahydroisoquinolin-4-yl or tetrahydroisoquinolin-6-yl, and the like), pyrrolo[3,2-c]pyridinyl (including, for example, pyrrolo[3,2-c]pyridin-2-yl or pyrrolo[3,2-c]pyridin-7-yl, and the like), benzopyranyl, thiazolyl, isothiazolyl, thiadiazolyl, benzothiazolyl, benzothienyl, and the derivatives thereof, or N-oxide or a protected derivative thereof.

“Hetereoarylalkyl” means an alkyl group substituted with one or two heteroaryl groups as defined herein.

“Heterocycloalkyl” means a saturated or partially unsaturated monovalent monocyclic group of 3 to 8 ring atoms or a saturated or partially unsaturated monovalent fused bicyclic group of 5 to 12 ring atoms in which one or more, for example one, two, three, or four ring heteroatoms independently selected from —O—, —S(O)_(n)— (n is 0, 1, or 2), —N═, —N(R^(y))— (where R^(y) is hydrogen, alkyl, hydroxy, alkoxy, acyl, or alkylsulfonyl), the remaining ring atoms being carbon. One or two ring carbon atoms may be replaced by a —C(O)—, —C(S)—, or —C(═NH)— group. Fused bicyclic radical includes bridged ring systems. Unless otherwise stated, the valency of the group may be located on any atom of any ring within the radical, valency rules permitting. In particular, when the point of valency is located on a nitrogen atom, R^(y) is absent. In another embodiment the term heterocycloalkyl includes, but is not limited to, azetidinyl, pyrrolidinyl, 2-oxopyrrolidinyl, 2,5-dihydro-1H-pyrrolyl, piperidinyl, 4-piperidonyl, morpholinyl, piperazinyl, 2-oxopiperazinyl, tetrahydropyranyl, 2-oxopiperidinyl, thiomorpholinyl, thiamorpholinyl, perhydroazepinyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, dihydropyridinyl, tetrahydropyridinyl, oxazolinyl, oxazolidinyl, isoxazolidinyl, thiazolinyl, thiazolidinyl, quinuclidinyl, isothiazolidinyl, octahydroindolyl, octahydroisoindolyl, decahydroisoquinolyl, tetrahydrofuryl, and tetrahydropyranyl, and the derivatives thereof and N-oxide or a protected derivative thereof.

“Heterocycloalkylalkyl” means an alkyl group, as defined herein, substituted with one or two heterocycloalkyl groups, as defined herein.

“Hydroxyalkyl” means an alkyl radical, as defined herein, substituted with at least one, for example one, two, or three, hydroxy groups, provided that if two hydroxy groups are present they are not both on the same carbon atom. Representative examples include, but are not limited to, hydroxymethyl, 2-hydroxyethyl, 2-hydroxypropyl, 3-hydroxypropyl, 1-(hydroxymethyl)-2-methylpropyl, 2-hydroxybutyl, 3-hydroxybutyl, 4-hydroxybutyl, 2,3-dihydroxypropyl, 1-(hydroxymethyl)-2-hydroxyethyl, 2,3-dihydroxybutyl, 3,4-dihydroxybutyl and 2-(hydroxymethyl)-3-hydroxypropyl, for example 2-hydroxyethyl, 2,3-dihydroxypropyl, or 1-(hydroxymethyl)-2-hydroxyethyl, and the like.

“Hydroxyamino” means a —NH(OH) group.

“Optional” or “optionally” means that the subsequently described event or circumstance may or may not occur, and that the description includes instances where said event or circumstance occurs and instances in which it does not. One of ordinary skill in the art would understand that with respect to any molecule described as containing one or more optional substituents, only sterically practical and/or synthetically feasible compounds are meant to be included. “Optionally substituted” refers to all subsequent modifiers in a term. So, for example, in the term “optionally substituted arylC₁₋₈ alkyl,” both the “C₁₋₈ alkyl” portion and the “aryl” portion of the molecule may or may not be substituted. A list of exemplary optional substitutions is presented below in the definition of “substituted.”

“Optionally substituted alkyl” means an alkyl radical, as defined herein, optionally substituted with one or more groups, for example one, two, three, four, or five groups, independently selected from alkylcarbonyl, alkenylcarbonyl, cycloalkylcarbonyl, alkylcarbonyloxy, alkenylcarbonyloxy, amino, alkylamino, dialkylamino, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, cyano, cyanoalkylaminocarbonyl, alkoxy, alkenyloxy, hydroxy, hydroxyalkoxy, carboxy, alkylcarbonylamino, alkylcarbonyloxy, alkyl-S(O)₀₋₂—, alkenyl-S(O)₀₋₂—, aminosulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl, alkylsulfonyl-NR^(c)— (where R^(c) is hydrogen, alkyl, optionally substituted alkenyl, optionally substituted alkynyl, hydroxy, alkoxy, alkenyloxy, or cyanoalkyl), alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkylaminoalkyloxy, dialkylaminoalkyloxy, alkoxycarbonyl, alkenyloxycarbonyl, alkoxycarbonylamino, alkylaminocarbonylamino, dialkylaminocarbonylamino, alkoxyalkyloxy, and —C(O)NR^(a)R^(b) (where R^(a) and R^(b) are independently hydrogen, alkyl, optionally substituted alkenyl, optionally substituted alkynyl, hydroxy, alkoxy, alkenyloxy, or cyanoalkyl).

“Optionally substituted alkenyl” means an alkenyl radical, as defined herein, optionally substituted with one or more groups, for example one, two, or three groups, independently selected from alkylcarbonyl, alkenylcarbonyl, cycloalkylcarbonyl, alkylcarbonyloxy, alkenylcarbonyloxy, amino, alkylamino, dialkylamino, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, cyano, cyanoalkylaminocarbonyl, alkoxy, alkenyloxy, hydroxy, hydroxyalkoxy, carboxy, alkylcarbonylamino, alkylcarbonyloxy, alkyl-S(O)₀₋₂—, alkenyl-S(O)₀₋₂—, aminosulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl, alkylsulfonyl-NR^(c)— (where R^(c) is hydrogen, optionally substituted alkyl, optionally substituted alkynyl, hydroxy, alkoxy, or alkenyloxy), alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkylaminoalkyloxy, dialkylaminoalkyloxy, alkoxycarbonyl, alkenyloxycarbonyl, alkoxycarbonylamino, alkylaminocarbonylamino, dialkylaminocarbonylamino, alkoxyalkyloxy, and —C(O)NR^(a)R^(b) (where R^(a) and R^(b) are independently hydrogen, optionally substituted alkyl, alkenyl, optionally substituted alkynyl, hydroxy, alkoxy, or alkenyloxy).

“Optionally substituted aryl” means an aryl group, as defined herein, which is optionally substituted with one, two, three, four, of five groups selected from halo, haloalkyl, haloalkoxy, hydroxy, lower alkyl, lower alkenyl, lower alkynyl, alkoxy, carboxy, carboxy ester, amino, alkylamino, dialkylamino, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted heteroaryl, —C(O)NR′R″ (where R′ is hydrogen or alkyl and R″ is hydrogen, alkyl, aryl, heteroaryl, or heterocycloalkyl), —NR′C(O)R″ (where R′ is hydrogen or alkyl and R″ is alkyl, aryl, heteroaryl, or heterocycloalkyl), and —NHS(O)₂R′ (where R′ is alkyl, aryl, or heteroaryl).

“Optionally substituted heteroaryl” means a heteroaryl group, as defined herein, optionally substituted with one, two, three, four, or five groups selected from halo, haloalkyl, haloalkoxy, lower alkyl, lower alkenyl, lower alkynyl, alkoxy, hydroxy, oxo (valency rules permitting), carboxy, carboxy ester, amino, alkylamino, dialkylamino, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, heteroaryl, optionally substituted aryl, —C(O)NR′R″ (where R′ is hydrogen or alkyl and R″ is hydrogen, alkyl, aryl, heteroaryl, or heterocycloalkyl), —NR′C(O)R″ (where R′ is hydrogen or alkyl and R″ is alkyl, aryl, heteroaryl, or heterocycloalkyl), and —NHS(O)₂R′ (where R′ is alkyl, aryl, or heteroaryl).

“Optionally substituted heterocycloalkyl” means a heterocycloalkyl, as defined herein, optionally substituted with one, two, three, four, or five groups selected from halo, haloalkyl, haloalkoxy, hydroxy, oxo, lower alkyl, lower alkenyl, lower alkynyl, alkoxy, optionally substituted cycloalkyl, heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, alkylaminoalkyl, dialkylaminoalkyl, carboxy, carboxy ester, —C(O)NR′R″ (where R′ is hydrogen or alkyl and R″ is hydrogen, alkyl, aryl, heteroaryl, or heterocycloalkyl), —NR′C(O)R″ (where R′ is hydrogen or alkyl and R″ is alkyl, aryl, heteroaryl, or heterocycloalkyl), amino, alkylamino, dialkylamino, and —NHS(O)₂R′ (where R′ is alkyl, aryl, or heteroaryl).

“Saturated bridged ring system” refers to a bicyclic or polycyclic ring system that is not aromatic. Such a system may contain isolated or conjugated unsaturation, but not aromatic or heteroaromatic rings in its core structure (but may have aromatic substitution thereon). For example, hexahydro-furo[3,2-b]furan, 2,3,3a,4,7,7a-hexahydro-1H-indene, 7-aza-bicyclo[2.2.1]heptane, and 1,2,3,4,4a,5,8,8a-octahydro-naphthalene are all included in the class “saturated bridged ring system.”

“Spirocyclyl” or “spirocyclic ring” refers to a ring originating from a particular annular carbon of another ring. For example, as depicted below, a ring atom of a saturated bridged ring system (rings C and C′), but not a bridgehead atom, can be a shared atom between the saturated bridged ring system and a spirocyclyl (ring D) attached thereto. A spirocyclyl can be carbocyclic or heteroalicyclic.

“Yield” for each of the reactions described herein is expressed as a percentage of the theoretical yield.

Definitions for the Compound of Formula 100

The terms used to describe the scope of formula 100 are defined in WO 2004/006846 (US Nat'l Stage application Ser. No. 10/522,004) which is herein incorporated by reference. For example “optionally substituted alkyl” for formula 100 has the meaning given in WO 2004/006846 (US Nat'l Stage application Ser. No. 10/522,004). Whenever a compound of formula 100 is described in this application, whether by structure or by use of the term “formula 100,” the terms used to describe that compound are defined by WO 2004/006846 (US Nat'l Stage application Ser. No. 10/522,004).

Other Definitions

“AKT inhibitor” includes, for example, LY294002, PKC 412, perifosine, compounds in Table 2a, compounds in Table 2b, and compounds described in WO 2006/071819 and WO05/117909. These references also describe in vitro assays that can be used to determine the inhibitory activity of AKT.

“Alkylating agent” includes, for example, one or more of the following: Chlorambucil, Chlormethine, Cyclophosphamide, Ifosfamide, Melphalan, Carmustine, Streptozocin, Fotemustine, Lomustine, Streptozocin, Carboplatin, Cisplatin, Oxaliplatin, BBR3464, Busulfan, Dacarbazine, Mechlorethamine, Procarbazine, Temozolomide, ThioTEPA, and Uramustine.

“Antibody” includes, for example, one or more of the following: an IGF1R antibody (including, for example, ^(α)IGF-1R A12 MoAb, 19D12, h7C10 and CP-751871), an EGFR antibody (including, for example, Cetuximab (Erbitux®) and Panitumumab), an ErbB2 antibody (including, for example, Trastuzumab (Herceptin®)), a VEGF antibody (including, for example, Bevacizumab (Avastin®)), an IgG1 antibody (including, for example, Ibritumomab (tiuxetan)), a CD20 antibody (including, for example, Rituximab and Tositumomab), a CD33 antibody (including, for example, Gemtuzumab and Gemtuzumab ozogamicin), and a CD52 antibody (including, for example, Alemtuzumab).

“Antimetabolite” include, for example, methotrexate, Pemetrexed, Raltitrexed, Cladribine, Clofarabine, Fludarabine, Mercaptopurine, Thioguanine, Capecitabine, Cytarabine, fluorouracil (administered with or without leucovorin or folinic acid), and Gemcitabine.

“Antimicrotubule agent” includes, for example, Vincristine, Vinblastine, Vinorelbine, Vinflunine, and Vindesine.

“Aromatase inhibitor” includes, for example, one or more of the following: Aminoglutethimide, Anastrozole (Arimidex®), Letrozole (Femara®), Exemestane (Aromasin®), and Formestane (Lentaron®).

“Cancer” refers to cellular-proliferative disease states, including but not limited to: Cardiac: sarcoma (angiosarcoma, fibrosarcoma, rhabdomyosarcoma, liposarcoma), myxoma, rhabdomyoma, fibroma, lipoma and teratoma; Lung: bronchogenic carcinoma (squamous cell, undifferentiated small cell, undifferentiated large cell, adenocarcinoma), alveolar (bronchiolar) carcinoma, bronchial adenoma, sarcoma, lymphoma, chondromatous hanlartoma, inesothelioma; Gastrointestinal: esophagus (squamous cell carcinoma, adenocarcinoma, leiomyosarcoma, lymphoma), stomach (carcinoma, lymphoma, leiomyosarcoma), pancreas (ductal adenocarcinoma, insulinoma, glucagonoma, gastrinoma, carcinoid tumors, vipoma), small bowel (adenocarcinoma, lymphoma, carcinoid tumors, Karposi's sarcoma, leiomyoma, hemangioma, lipoma, neurofibroma, fibroma), large bowel (adenocarcinoma, tubular adenoma, villous adenoma, hamartoma, leiomyoma); Genitourinary tract: kidney (adenocarcinoma, Wilm's tumor [nephroblastoma], lymphoma, leukemia), bladder and urethra (squamous cell carcinoma, transitional cell carcinoma, adenocarcinoma), prostate (adenocarcinoma, sarcoma), testis (seminoma, teratoma, embryonal carcinoma, teratocarcinoma, choriocarcinoma, sarcoma, interstitial cell carcinoma, fibroma, fibroadenoma, adenomatoid tumors, lipoma); Liver: hepatoma (hepatocellular carcinoma), cholangiocarcinoma, hepatoblastoma, angiosarcoma, hepatocellular adenoma, hemangioma; Bone: osteogenic sarcoma (osteosarcoma), fibrosarcoma, malignant fibrous histiocytoma, chondrosarcoma, Ewing's sarcoma, malignant lymphoma (reticulum cell sarcoma), multiple myeloma, malignant giant cell tumor chordoma, osteochronfroma (osteocartilaginous exostoses), benign chondroma, chondroblastoma, chondromyxofibroma, osteoid osteoma and giant cell tumors; Nervous system: skull (osteoma, hemangioma, granuloma, xanthoma, osteitis deformians), meninges (meningioma, meningiosarcoma, gliomatosis), brain (astrocytoma, medulloblastoma, glioma, ependymoma, germinoma [pinealoma], glioblastorna multiform, oligodendroglioma, schwannoma, retinoblastoma, congenital tumors), spinal cord neurofibroma, meningioma, glioma, sarcoma); Gynecological: uterus (endometrial carcinoma), cervix (cervical carcinoma, pre-tumor cervical dysplasia), ovaries (ovarian carcinoma [serous cystadenocarcinoma, mucinous cystadenocarcinoma, unclassified carcinoma], granulosa-thecal cell tumors, Sertoli-Leydig cell tumors, dysgerminoma, malignant teratoma), vulva (squamous cell carcinoma, intraepithelial carcinoma, adenocarcinoma, fibrosarcoma, melanoma), vagina (clear cell carcinoma, squamous cell carcinoma, botryoid sarcoma (embryonal rhabdomyosarcoma], fallopian tubes (carcinoma); Hematologic: blood (myeloid leukemia [acute and chronic], acute lymphoblastic leukemia, chronic lymphocytic leukemia, myeloproliferative diseases, multiple myeloma, myelodysplastic syndrome), Hodgkin's disease, non-Hodgkin's lymphoma [malignant lymphoma]; Skin: malignant melanoma, basal cell carcinoma, squamous cell carcinoma, Karposi's sarcoma, moles dysplastic nevi, lipoma, angioma, dermatofibroma, keloids, psoriasis; Adrenal Glands: neuroblastoma; and breast cancer. Thus, the term “cancerous cell” as provided herein, includes a cell afflicted by any one of the above-identified conditions.

“Chemotherapeutic agent” includes, but is not limited to, an AKT inhibitor, an alkylating agent, an antimetabolite, an antimicrotubule agent, an aromatase inhibitor, a c-KIT inhibitor, a cMET inhibitor, an EGFR inhibitor, an ErbB2 inhibitor, a Flt-3 inhibitor, an HSP90 inhibitor, an IGF1R inhibitor, a platin, a Raf inhibitor, rapamycin, a Rapamycin analogue, a Receptor Tyrosine Kinase inhibitor, a taxane, a topoisomerase inhibitor, a SRC and/or ABL kinase inhibitor, and a VEGFR inhibitor. A pharmaceutically acceptable salt, solvate, and/or hydrate of a chemotherapeutic agent can be prepared by one of ordinary skill in the art and such salt, solvate, and/or hydrates thereof can be used to practice the invention.

“c-KIT inhibitor” includes, for example, imatinib, sunitinib, nilotinib, AMG 706, sorafenib, compounds in Table 3b, compounds in Table 3c, compounds in Table 8, compounds in Table 9, and compounds described in WO 2006/108059, WO/2005/020921, WO/2006/033943, and WO 2005/030140.

“cMET inhibitor” includes, for example, compounds in Table 3a, compounds in Table 3b, compounds in Table 3c, compounds described in WO06/108059, WO 2006/014325, and WO 2005/030140.

“EGFR inhibitor” includes, for example, one or more of the following: pelitinib, lapatinib (Tykerb®), gefitinib (Iressa®), erlotinib (Tarceva®), Zactima (ZD6474, vandetinib), AEE788 and HKI-272, EKB-569, CI-1033, N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, compounds in Table 4, compounds in Table 7, and compounds described in WO 2004/006846 and WO 2004/050681.

“ErbB2 inhibitor” includes, for example, lapatinib (GW572016), PKI-166, canertinib, CI-1033, HKI272, and EKB-569.

“Flt-3 inhibitor” includes, for example, CEP-701, PKC 412, MLN518, sunitinib, sorafenib, compounds in Table 3a, compounds in Table 3b, compounds in Table 3c, compounds in Table 9, and compounds described in WO 2006/108059, WO/2006/033943, WO 2006/014325, and WO 2005/030140.

“Hormone therapy” or “hormonal therapy” includes, for example, treatment with one or more of the following: steroids (e.g. dexamethasone), finasteride, tamoxifen, and an aromatase inhibitor.

“HSP90 inhibitor” includes, for example, 17-AAG, 17-DMAG, Geldanamycin, 5-(2,4-dihydroxy-5-isopropylphenyl)-N-ethyl-4-(4-(morpholinomethyl)phenyl)isoxazole-3-carboxamide [NVP-AUY922 (VER 52296)], 6-chloro-9-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-9H-purin-2-amine (CNF2024, also named BIIB021), compounds disclosed in WO2004072051 (which is herein incorporated by reference), compounds disclosed in WO2005028434 (which is herein incorporated by reference), compounds disclosed in WO2007035620 (which is herein incorporated by reference) and compounds disclosed in WO2006091963 (which is herein incorporated by reference).

“IGF1R inhibitor” includes, for example, Tyrphostin AG 1024, compounds in Table 5a, compounds in Table 5b, and compounds described in WO06/074057.

“Kinase-dependent diseases or conditions” refer to pathologic conditions that depend on the activity of one or more lipid kinases. Kinases either directly or indirectly participate in the signal transduction pathways of a variety of cellular activities including proliferation, adhesion, migration, differentiation and invasion. Diseases associated with kinase activities include tumor growth, the pathologic neovascularization that supports solid tumor growth, and associated with other diseases where excessive local vascularization is involved such as ocular diseases (diabetic retinopathy, age-related macular degeneration, and the like) and inflammation (psoriasis, rheumatoid arthritis, and the like).

While not wishing to be bound to theory, phosphatases can also play a role in “kinase-dependent diseases or conditions” as cognates of kinases; that is, kinases phosphorylate and phosphatases dephosphorylate, for example lipid substrates. Therefore compounds of the invention, while modulating kinase activity as described herein, may also modulate, either directly or indirectly, phosphatase activity. This additional modulation, if present, may be synergistic (or not) to activity of compounds of the invention toward a related or otherwise interdependent kinase or kinase family. In any case, as stated previously, the compounds of the invention are useful for treating diseases characterized in part by abnormal levels of cell proliferation (i.e. tumor growth), programmed cell death (apoptosis), cell migration and invasion and angiogenesis associated with tumor growth.

“Metabolite” refers to the break-down or end product of a compound or its salt produced by metabolism or biotransformation in the animal or human body; for example, biotransformation to a more polar molecule such as by oxidation, reduction, or hydrolysis, or to a conjugate (see Goodman and Gilman, “The Pharmacological Basis of Therapeutics” 8.sup.th Ed., Pergamon Press, Gilman et al. (eds), 1990 for a discussion of biotransformation). As used herein, the metabolite of a compound of the invention or its salt may be the biologically active form of the compound in the body. In one example, a prodrug may be used such that the biologically active form, a metabolite, is released in vivo. In another example, a biologically active metabolite is discovered serendipitously, that is, no prodrug design per se was undertaken. An assay for activity of a metabolite of a compound of the present invention is known to one of skill in the art in light of the present disclosure.

“Patient” for the purposes of the present invention includes humans and other animals, particularly mammals, and other organisms. Thus the methods are applicable to both human therapy and veterinary applications. In another embodiment the patient is a mammal, and in another embodiment the patient is human.

A “pharmaceutically acceptable salt” of a compound means a salt that is pharmaceutically acceptable and that possesses the desired pharmacological activity of the parent compound. It is understood that the pharmaceutically acceptable salts are non-toxic. Additional information on suitable pharmaceutically acceptable salts can be found in Remington's Pharmaceutical Sciences, 17^(th) ed., Mack Publishing Company, Easton, Pa., 1985, which is incorporated herein by reference or S. M. Berge, et al., “Pharmaceutical Salts,” J. Pharm. Sci., 1977; 66:1-19 both of which are incorporated herein by reference.

Examples of pharmaceutically acceptable acid addition salts include those formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like; as well as organic acids such as acetic acid, trifluoroacetic acid, propionic acid, hexanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, 3-(4-hydroxybenzoyl)benzoic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, 1,2-ethanedisulfonic acid, 2-hydroxyethanesulfonic acid, benzenesulfonic acid, 4-chlorobenzenesulfonic acid, 2-naphthalenesulfonic acid, 4-toluenesulfonic acid, camphorsulfonic acid, glucoheptonic acid, 4,4′-methylenebis-(3-hydroxy-2-ene-1-carboxylic acid), 3-phenylpropionic acid, trimethylacetic acid, tertiary butylacetic acid, lauryl sulfuric acid, gluconic acid, glutamic acid, hydroxynaphthoic acid, salicylic acid, stearic acid, muconic acid, p-toluenesulfonic acid, and salicylic acid and the like.

Examples of a pharmaceutically acceptable base addition salts include those formed when an acidic proton present in the parent compound is replaced by a metal ion, such as sodium, potassium, lithium, ammonium, calcium, magnesium, iron, zinc, copper, manganese, aluminum salts and the like. Preferable salts are the ammonium, potassium, sodium, calcium, and magnesium salts. Salts derived from pharmaceutically acceptable organic non-toxic bases include, but are not limited to, salts of primary, secondary, and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines and basic ion exchange resins. Examples of organic bases include isopropylamine, trimethylamine, diethylamine, triethylamine, tripropylamine, ethanolamine, 2-dimethylaminoethanol, 2-diethylaminoethanol, dicyclohexylamine, lysine, arginine, histidine, caffeine, procaine, hydrabamine, choline, betaine, ethylenediamine, glucosamine, methylglucamine, theobromine, purines, piperazine, piperidine, N-ethylpiperidine, tromethamine, N-methylglucamine, polyamine resins, and the like. Exemplary organic bases are isopropylamine, diethylamine, ethanolamine, trimethylamine, dicyclohexylamine, choline, and caffeine.

“Platin,” and “platin-containing agent” include, for example, cisplatin, carboplatin, and oxaliplatin.

“Prodrug” refers to compounds that are transformed (typically rapidly) in vivo to yield the parent compound of the above formulae, for example, by hydrolysis in blood. Common examples include, but are not limited to, ester and amide forms of a compound having an active form bearing a carboxylic acid moiety. Examples of pharmaceutically acceptable esters of the compounds of this invention include, but are not limited to, alkyl esters (for example with between about one and about six carbons) the alkyl group is a straight or branched chain. Acceptable esters also include cycloalkyl esters and arylalkyl esters such as, but not limited to benzyl. Examples of pharmaceutically acceptable amides of the compounds of this invention include, but are not limited to, primary amides, and secondary and tertiary alkyl amides (for example with between about one and about six carbons). Amides and esters of the compounds of the present invention may be prepared according to conventional methods. A thorough discussion of prodrugs is provided in T. Higuchi and V. Stella, “Pro-drugs as Novel Delivery Systems,” Vol 14 of the A.C.S. Symposium Series, and in Bioreversible Carriers in Drug Design, ed. Edward B. Roche, American Pharmaceutical Association and Pergamon Press, 1987, both of which are incorporated herein by reference for all purposes.

“Raf inhibitor” includes, for example, sorafenib, RAF 265 (CHIR 265), compounds in Table 6, and compounds described in WO 2005/112932. These references also describe in vitro assays that can be used to determine the inhibitory activity of RAF.

“Rapamycin analogue” includes for example, CCI-779, AP23573, RAD 001, TAFA 93, and compounds described in WO 2004/101583 and U.S. Pat. No. 7,160,867 which are each incorporated herein by reference in their entireties.

“Receptor Tyrosine Kinase inhibitor” includes, for example, inhibitors of AKT, EGFR, ErbB2, IGF1R, KIT, Met, Raf, and VEGFR2. Examples of receptor tyrosine kinase inhibitors can be found in WO 2006/108059 (US Nat'l Stage application Ser. No. 11/910,720), WO 2006/074057 (US Nat'l Stage application Ser. No. 11/722,719), WO 2006/071819 (US Nat'l Stage application Ser. No. 11/722,291), WO 2006/014325 (US Nat'l Stage application Ser. No. 11/571,140), WO 2005/117909 (US Nat'l Stage application Ser. No. 11/568,173), WO 2005/030140 (US Nat'l Stage application Ser. No. 10/573,336), WO 2004/050681 US Nat'l Stage application Ser. No. 10/533,555), WO 2005/112932 (US Nat'l Stage application Ser. No. 11/568,789), and WO 2004/006846 (US Nat'l Stage application Ser. No. 10/522,004), each of which is incorporated herein by reference for all purposes. In particular, the applications cited in this paragraph are incorporated for the purpose of providing specific examples and generic embodiments (and the definitions associated with the terms used in the embodiments) of compounds that are useful in the practice of the invention. These references also describe in vitro assays useful in the practice of this invention.

“Taxane” includes, for example, one or more of the following: Paclitaxel (Taxol®) and Docetaxel (Taxotere®).

“Therapeutically effective amount” is an amount of a compound of the invention, that when administered to a patient, ameliorates a symptom of the disease. The amount of a compound of the invention which constitutes a “therapeutically effective amount” will vary depending on the compound, the disease state and its severity, the age of the patient to be treated, and the like. The therapeutically effective amount can be determined routinely by one of ordinary skill in the art having regard to their knowledge and to this disclosure.

“Topoisomerase inhibitor” includes, for example, one or more of the following: amsacrine, camptothecin, etoposide, etoposide phosphate, exatecan, irinotecan, lurtotecan, and teniposide, and topotecan.

“Treating” or “treatment” of a disease, disorder, or syndrome, as used herein, includes (i) preventing the disease, disorder, or syndrome from occurring in a human, i.e. causing the clinical symptoms of the disease, disorder, or syndrome not to develop in an animal that may be exposed to or predisposed to the disease, disorder, or syndrome but does not yet experience or display symptoms of the disease, disorder, or syndrome; (ii) inhibiting the disease, disorder, or syndrome, i.e., arresting its development; and (iii) relieving the disease, disorder, or syndrome, i.e., causing regression of the disease, disorder, or syndrome. As is known in the art, adjustments for systemic versus localized delivery, age, body weight, general health, sex, diet, time of administration, drug interaction and the severity of the condition may be necessary, and will be ascertainable with routine experimentation by one of ordinary skill in the art.

“SRC and/or ABL kinase inhibitor” includes, for example, dasatinib, imatinib (Gleevec®), and compounds described in WO 2006/074057.

“VEGFR inhibitor” includes, for example, one or more of the following: VEGF Trap, ZD6474 (vandetanib, Zactima), sorafenib, Angiozyme, AZD2171 (cediranib), pazopanib, sorafenib, axitinib, SU5416 (semaxanib), PTK787 (vatalanib), AEE778, RAF 265, sunitinib (Sutent), N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, compounds in Table 7, and compounds described in WO 2004/050681 and WO 2004/006846.

Embodiments of the Invention

The following paragraphs present a number of embodiments of compounds of the invention. In each instance, the embodiment includes both the recited compounds as well as individual isomers and mixtures of isomers. In addition, in each instance, the embodiment optionally includes the pharmaceutically acceptable salts, hydrates, and/or solvates of the recited compounds and any individual isomers or mixture of isomers thereof.

For each of the following embodiments, the Compound of Formula I can, for example, be of Formula I(a) or be selected from a Compound in Table 1.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, where growth and/or survival of tumor cells of the cancer is enhanced, at least in part, by the activity of PI3K; in combination with one or more treatments selected from surgery, one or more chemotherapeutic agents, one or more hormone therapies, one or more antibodies, one or more immunotherapies, radioactive iodine therapy, and radiation.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, one or more chemotherapeutic agents, one or more hormone therapies, one or more antibodies, one or more immunotherapies, radioactive iodine therapy, and radiation; where the cancer is selected from breast cancer, colon cancer, rectal cancer, endometrial cancer, gastric carcinoma (including gastrointestinal carcinoid tumors and gastrointestinal stromal tumors), glioblastoma, hepatocellular carcinoma, small cell lung cancer, non-small cell lung cancer (NSCLC), melanoma, ovarian cancer, cervical cancer, pancreatic cancer, prostate carcinoma, acute myelogenous leukemia (AML), chronic myelogenous leukemia (CML), non-Hodgkin's lymphoma, and thyroid carcinoma. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, one or more chemotherapeutic agents, one or more hormone therapies, one or more antibodies, one or more immunotherapies, radioactive iodine therapy, and radiation; where the cancer is selected from prostate cancer, NSCLC, ovarian cancer, cervical cancer, breast cancer, colon cancer, rectal cancer, and glioblastoma. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, one or more chemotherapeutic agents, one or more hormone therapies, one or more antibodies, one or more immunotherapies, radioactive iodine therapy, and radiation; where the cancer is selected from NSCLC, breast cancer, prostate cancer, glioblastoma, and ovarian cancer.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or more chemotherapeutic agents.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents independently selected from rapamycin, a rapamycin analogue, an alkylating agent, a taxane, a platin, an EGFR inhibitor, and an ErbB2 inhibitor. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents independently selected from rapamycin, temozolomide, paclitaxel, docetaxel, carboplatin, cisplatin, oxaliplatin, gefitinib (Iressa®), erlotinib (Tarceva®), Zactima (ZD6474), HKI-272, pelitinib, canertinib, a compound selected from Table 4, a compound in Table 7, and lapatinib. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents independently selected from rapamycin, temozolomide, paclitaxel, docetaxel, carboplatin, trastuzumab, erlotinib, N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, a compound in Table 7, and lapatinib. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents independently selected from rapamycin, paclitaxel, carboplatin, erlotinib, and N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta-[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents independently selected from a platin and a taxane. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents independently selected from carboplatin, cisplatin, oxaliplatin, and paclitaxel.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is an AKT inhibitor. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is an AKT inhibitor selected from perifosine, PKC 412, a compound in Table 2a, and a compound in Table 2b.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is a cMET inhibitor. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is a cMET inhibitor selected from a compound in Table 3a, a compound in Table 3b, and a compound in Table 3c.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is an EGFR inhibitor. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is an EGFR inhibitor selected from lapatinib (Tykerb®), gefitinib (Iressa®), erlotinib (Tarceva®), Zactima (ZD6474), AEE788, HKI-272, EKB-569, CI 1033, a compound selected from Table 4, and a compound in Table 7. In another embodiment, In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is an EGFR inhibitor selected from lapatinib (Tykerb®), gefitinib (Iressa®), erlotinib (Tarceva®), Zactima (ZD6474), AEE788, HKI-272, EKB-569, CI 1033, N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, and N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is an ErbB2 inhibitor. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is an ErbB2 inhibitor selected from lapatinib, EKB-569, HKI272, CI 1033, PKI-166, and a compound selected from Table 4.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is an HSP90 inhibitor. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is an HSP90 inhibitor selected from 17-AAG, 17-DMAG, Geldanamycin, and CNF2024. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is an HSP90 inhibitor selected from 17-AAG, 17-DMAG, and Geldanamycin.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is an IGF1R inhibitor. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is an IGF1R inhibitor selected from Table 5a and Table 5b.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is a Raf inhibitor. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is a Raf inhibitor selected from sorafenib, RAF 265 (CHIR-265), and a compound in Table 6.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is a VEGFR inhibitor. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is a VEGFR inhibitor selected from VEGF Trap, ZD6474 (Zactima), cediranib (AZ2171), pazopanib, sunitinib, sorafenib, axitinib, AEE788, RAF 265 (CHIR-265), a compound selected from Table 4, and a compound selected from Table 7.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is a cKIT inhibitor. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is a cKIT inhibitor selected from imatinib, sunitinib, nilotinib, AMG 706, sorafenib, a compound in Table 3b, a compound in Table 3c, a compound in Table 8, and a compound in Table 9.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is a FLT3 inhibitor. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is a FLT3 inhibitor selected from CEP-701, PKC 412, sunitinib, MLN518, sunitinib, sorafenib, a compound in Table 3a, a compound in Table 3b, a compound in Table 3c, and a compound in Table 9.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from rapamycin, a rapamycin analogue, PI103, and SF 1126. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from rapamycin, CCI-779, AP23573, RAD 001, TAFA 93, PI103, and SF 1126. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is rapamycin.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is of formula 100:

where q is 1, 2, or 3; E is —NR⁹—, —O—, or absent and Y is —CH₂CH₂—, —CH₂—, or absent provided that when E is —NR⁹— or —O—, then Y is —CH₂CH₂—; R² is selected from halogen, trihalomethyl, —CN, —NO₂, —OR³, and lower alkyl; R⁸ is selected from —H, lower alkyl, —C(O)OR³, —C(O)N(R³)R⁴, —SO₂R⁴, and —C(O)R³; R⁹ is hydrogen or lower alkyl; R³ is hydrogen or R⁴; R⁴ is selected from lower alkyl, aryl, lower arylalkyl, heterocyclyl, and lower heterocyclylalkyl; or R³ and R⁴, when taken together with a common nitrogen to which they are attached, form a five- to seven-membered heterocyclyl, said five- to seven-membered heterocyclyl optionally containing one or more additional heteroatom selected from N, O, S, and P; or a single geometric isomer, stereoisomer, racemate, enantiomer, or diastereomer, thereof and optionally as a pharmaceutically acceptable salt, additionally optionally as a solvate, and additionally as a hydrate thereof. The terms used to describe the scope of formula 100 are defined in WO 2004/006846 (US Nat'l Stage application Ser. No. 10/522,004) which is herein incorporated by reference. Whenever a compound of formula 100 is described in this application, whether by structure or by use of the term “formula 100,” the terms used to describe that compound are defined by WO 2004/006846 (US Nat'l Stage application Ser. No. 10/522,004). In particular, “alkyl” in formula 100 is intended to include linear, branched, or cyclic hydrocarbon structures and combinations thereof, inclusively; “lower alkyl” means alkyl groups of from one to six carbon atoms. “Aryl” in formula 100 means an aromatic six- to fourteen-membered carbocyclic rings which include, for example, benzene, naphthalene, indane, tetralin, fluorene and the like. “Lower arylalkyl” in formula 100 means a residue in which an aryl moiety is attached to a parent structure via one of an alkylene, alkenylene, or alkynylene radical where the “alkyl” portion of the group has one to six carbons; examples include benzyl, phenethyl, phenylvinyl, phenylallyl and the like. In formula 100, “heterocyclyl” means a stable monocyclic, bicyclic or tricyclic three- to fifteen-membered ring radical (including fused or bridged ring systems) that consists of carbon atoms and from one to five heteroatoms selected from the group consisting of nitrogen, phosphorus, oxygen and sulfur where the nitrogen, phosphorus, carbon and sulfur atoms in the heterocyclyl radical may be optionally oxidized to various oxidation states and the nitrogen atom may be optionally quaternized; and the ring radical may be partially or fully saturated or aromatic. “Lower heterocyclylalkyl” means a residue in which a heterocyclyl is attached to a parent structure via one of an alkylene, alkenylene, and alkynylene radical having one to six carbons.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 2a. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a), in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 2a. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 2a.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 2b. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a), in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 2b. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 2b.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 3a. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a), in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 3a. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 3a.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 3b. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a), in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 3b. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 3b.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 3c. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a), in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 3c. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 3c.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 4. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a), in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 4. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 4.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, or N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a) in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, or N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, or N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta-[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a) in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta-[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is N-(3,4-dichloro-2-fluorophenyl)-7-({[3aR,5r,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 5ac. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a), in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 5a. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 5a.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 5b. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a), in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 5b. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 5b.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 6. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a), in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 6. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 6.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 7. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a), in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 7. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 7.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 8. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a), in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 8. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 8.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 9. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a), in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 9. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1, in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agents is selected from a compound in Table 9.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agent is paclitaxel.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agent is rapamycin.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agent is carboplatin.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agent is erlotinib.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is one or two chemotherapeutic agents where one of the chemotherapeutic agent is lapatinib.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is one or two antibodies where one of the antibodies is trastuzumab.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is one or two antibodies where one of the antibodies is cetuximab.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is one or two antibodies where one of the antibodies is panitumumab.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is one or two antibodies where one of the antibodies is bevacizumab.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is radiation. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a) in combination with a treatment where the treatment is radiation. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is radiation.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two antibodies. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two antibodies independently selected from an IGF1R antibody (including, for example, ^(α)IGF-1R A12 MoAb, ^(α)IGF-1R 19D12 MoAb, ^(α)IGF-1R h7C10 MoAb and ^(α)IGF-1R CP-751871 MoAb), Alemtuzumab, Bevacizumab (Avastin®), Gemtuzumab, Gemtuzumab ozogamicin, Ibritumomab tiuxetan, Panitumumab, Rituximab, Tositumomab, Omnitarg (pertuzimab), an anti-ErbB2 antibodies (including trastuzumab (Herceptin®)), and an anti-EGFR antibodies (including, for example, cetuximab (Erbitux), panitumumab, nimotuzumab, and EMD72000)).

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a) in combination with a treatment where the treatment is one or two antibodies. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a) in combination with a treatment where the treatment is one or two antibodies independently selected from an IGF1R antibody (including, for example, ^(α)IGF-1R A12 MoAb, ^(α)IGF-1R 19D12 MoAb, ^(α)IGF-1R h7C10 MoAb and ^(α)IGF-1R CP-751871 MoAb), Alemtuzumab, Bevacizumab (Avastin®), Gemtuzumab, Gemtuzumab ozogamicin, Ibritumomab tiuxetan, Panitumumab, Rituximab, Tositumomab, Omnitarg (pertuzimab), an anti-ErbB2 antibodies (including trastuzumab (Herceptin®)), and an anti-EGFR antibodies (including, for example, cetuximab (Erbitux), panitumumab, nimotuzumab, and EMD72000)).

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is one or two antibodies. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is one or two antibodies independently selected from an IGF1R antibody (including, for example, ^(α)IGF-1R A12 MoAb, ^(α)IGF-1R 19D12 MoAb, ^(α)IGF-1R h7C10 MoAb and ^(α)IGF-1R CP-751871 MoAb), Alemtuzumab, Bevacizumab (Avastin®), Gemtuzumab, Gemtuzumab ozogamicin, Ibritumomab tiuxetan, Panitumumab, Rituximab, Tositumomab, Omnitarg (pertuzimab), an anti-ErbB2 antibodies (including trastuzumab (Herceptin®)), and an anti-EGFR antibodies (including, for example, cetuximab (Erbitux), panitumumab, nimotuzumab, and EMD72000)).

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or more chemotherapeutic agents where one of the chemotherapeutic agent is temozolomide. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a) in combination with a treatment where the treatment is one or more chemotherapeutic agents where one of the chemotherapeutic agent is temozolomide. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is one or more chemotherapeutic agents where one of the chemotherapeutic agent is temozolomide.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is surgery. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a) in combination with a treatment where the treatment is surgery. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is surgery.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two hormone therapies. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I or I(a), as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two hormone therapies independently selected from tamoxifen, Toremifene (Fareston), Fulvestrant (Faslodex), Megestrol acetate (Megace), ovarian ablation, Raloxifene, a luteinizing hormone-releasing hormone (LHRH) analog (including goserelin and leuprolide), Megestrol acetate (Megace), and one or more aromatase inhibitors. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I or I(a), as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two hormone therapies where one of the hormone therapies is an aromatase inhibitor selected from letrozole (Femara), anastrozole (Arimidex), and exemestane (Aromasin). In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I or I(a), as defined in the Summary of the Invention, in combination with a treatment where the treatment is one or two hormone therapies independently selected from tamoxifen and an aromatase inhibitor.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where the treatment is one or two hormone therapies. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where one of the treatments is one or two hormone therapies independently selected from tamoxifen, Toremifene (Fareston), Fulvestrant (Faslodex), Megestrol acetate (Megace), ovarian ablation, Raloxifene, a luteinizing hormone-releasing hormone (LHRH) analog (including goserelin and leuprolide), Megestrol acetate (Megace), and one or two aromatase inhibitors. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where one of the treatments is one or two hormone therapies where one of the hormone therapies is an aromatase inhibitors selected from letrozole (Femara), anastrozole (Arimidex), and exemestane (Aromasin). In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where one of the treatments is one or two hormone therapies independently selected from tamoxifen and an aromatase inhibitor.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with a treatment where one of the treatments is one antibody selected from an EGFR antibody and an ErbB2 antibody, or the treatment is one or two chemotherapeutic agents independently selected from a rapamycin, rapamycin analogue, an alkylating agent, a taxane, a platin, an EGFR inhibitor, and an ErbB2 inhibitor. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I according to Formula I(a) in combination with a treatment where one of the treatments is one antibody selected from an EGFR antibody and an ErbB2 antibody, or the treatment is one or two chemotherapeutic agents independently selected from rapamycin, a rapamycin analogue, an alkylating agent, a taxane, a platin, an EGFR inhibitor, and an ErbB2 inhibitor. In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I selected from Table 1 in combination with a treatment where one of the treatments is one antibody selected from an EGFR antibody and an ErbB2 antibody, or the treatment is one or two chemotherapeutic agents independently selected from rapamycin, a rapamycin analogue, an alkylating agent, a taxane, a platin, an EGFR inhibitor, and an ErbB2 inhibitor.

In another embodiment, the invention is directed to a method of treating acute myelogenous leukemia (AML) which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from bone marrow or peripheral blood stem cell transplantation, radiation, one or two antibodies, and one or two chemotherapeutic agents. In another embodiment, the invention is directed to a method of treating acute myelogenous leukemia (AML) which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or t treatments where one of the treatments is one antibody selected from Gemtuzumab ozogamicin (Mylotarg), ^(α)IGF-1R A12 MoAb, ^(α)IGF-1R 19D12 MoAb, ^(α)IGF-1R h7C10 MoAb, ^(α)IGF-1R CP-751871 MoAb and trastuzumab. In another embodiment, the invention is directed to a method of treating acute myelogenous leukemia (AML) which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents selected from Imatinib (i.e. Gleevec®), PKC 412, CEP-701, daunorubicin, doxorubicin, cytarabine (ara-C), an anthracycline drug such as daunorubicin or idarubicin (Daunomycin, Idamycin), 6-thioguanine, and a granulocyte colony-stimulating factor (such as Neupogen or Leukine).

In another embodiment, the invention is directed to a method of treating chronic myelogenous leukemia (CML) which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from bone marrow or peripheral blood stem cell transplantation, radiation, one or two chemotherapeutic agents, immunotherapy, and one or two antibodies. In another embodiment, the invention is directed to a method of treating chronic myelogenous leukemia (CML) which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two of the chemotherapeutic agents selected from Imatinib (i.e. Gleevec®), PKC 412, hydroxyurea (Hydrea), cytosine, cytosine arabinoside, dasatinib, AMN107, VX680 (MK0457), and cytarabine (ara-C). In another embodiment, the invention is directed to a method of treating chronic myelogenous leukemia (CML) which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents selected from Imatinib (i.e. Gleevec®) and dasatinib. In another embodiment, the invention is directed to a method of treating chronic myelogenous leukemia (CML) which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is immunotherapy and the immunotherapy is interferon therapy such as interferon-α.

In another embodiment, the invention is directed to a method of treating prostate cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery (including cryosurgery), radiation, one or two chemotherapeutic agents, one or two antibodies, and one or two hormone therapies. In another embodiment, the invention is directed to a method of treating prostate cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is an antibody selected from ^(α)IGF-1R A12 MoAb, ^(α)IGF-1R 19D12 MoAb, ^(α)IGF-1R h7C10 MoAb, and ^(α)IGF-1R CP-751871 MoAb. In another embodiment, the invention is directed to a method of treating prostate cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two of the chemotherapeutic agents independently selected from rapamycin, mitoxantrone, prednisone, docetaxel (Taxotere), doxorubicin, etoposide, vinblastine, paclitaxel, and carboplatin. In another embodiment, the invention is directed to a method of treating prostate cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two of the hormone therapy indepependently selected from androgen deprivation therapy and androgen suppression therapy. In another embodiment, the invention is directed to a method of treating prostate cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents where one of the chemotherapeutic agents is a taxanes. In another embodiment, the invention is directed to a method of treating prostate cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents where one of the chemotherapeutic agents is rapamycin.

In another embodiment, the invention is directed to a method of treating melanoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, radiation, one or two immunotherapies, one or two hormone therapies, and one or two chemotherapeutic agents. In another embodiment, the invention is directed to a method of treating melanoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from an alkylating agent, a taxane, a platin, and a Raf inhibitor. In another embodiment, the invention is directed to a method of treating melanoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from sorafenib, Paclitaxel (Taxol®), Docetaxel (Taxotere®), dacarbazine, rapamycin, imatinib mesylate (Gleevec®), sorafenib, cisplatin, carboplatin, dacarbazine (DTIC), carmustine (BCNU), vinblastine, temozolomide (Temodar), Melphalan, and imiquimod (Aldara). In another embodiment, the invention is directed to a method of treating melanoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two immunotherapies independently selected from ipilimumab, interferon-alpha and interleukin-2. In another embodiment, the invention is directed to a method of treating melanoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is hormone therapy where the hormone therapy is tamoxifen.

In another embodiment, the invention is directed to a method of treating colon or rectal cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, radiation, one or two antibodies, and one or two chemotherapeutic agents. In another embodiment, the invention is directed to a method of treating colon or rectal cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is surgery selected from local excision, electrofulguration, segmental colon resection, polypectomy, local transanal resection, low anterior resection, abdominoperineal resection, and pelvic exenteration. In another embodiment, the invention is directed to a method of treating colon or rectal cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from a platinum-containing compound (including cisplatin, oxaliplatin, and carboplatin), 5-fluorouracil (5-FU), leucovorin, capecitabine (Xeloda), irinotecan (Camptosar), FOLFOX (Folinic acid, 5-FU, Oxaliplatin), and leucovorin. In another embodiment, the invention is directed to a method of treating colon or rectal cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two antibodies independently selected from cetuximab (Erbitux) and bevacizumab (Avastin).

In another embodiment, the invention is directed to a method of treating pancreatic cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, radiation, one or two antibodies, and one or two chemotherapeutic agents. In another embodiment, the invention is directed to a method of treating pancreatic cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is selected from one or two chemotherapeutic agents independently selected from platinum-containing compound (including cisplatin, oxaliplatin, and carboplatin), 5-fluorouracil (5-FU), gemcitabine, a taxane (including paclitaxel and docetaxel), topotecan, irinotecan, capecitabine, streptozocin, erlotinib (Tarceva), leucovorin, and capecitabine (Xeloda). In another embodiment, the invention is directed to a method of treating pancreatic cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is an antibody where the antibody is cetuximab.

In another embodiment, the invention is directed to a method of treating breast cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, radiation, one or two chemotherapeutic agents, one or two hormone therapies, and one or two antibodies. In another embodiment, the invention is directed to a method of treating breast cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two of the chemotherapeutic agents independently selected from lapatinib (Tykerb®), Paclitaxel (Taxol®), docetaxel, capecitabine, Cyclophosphamide (Cytoxan), CMF (cyclophosphamide, fluoruracil, and methotrexate), methotrexate, fluorouracil, doxorubicin, epirubicin, gemcitabine, carboplatin (Paraplatin), cisplatin (Platinol), vinorelbine (Navelbine), capecitabine (Xeloda), pegylated liposomal doxorubicin (Doxil), albumin-bound paclitaxel (Abraxane), AC (adriamycin and Cyclophosphamide), adriamyclin, and pamidronate or zoledronic acid (to treat bone weakness). In another embodiment, the invention is directed to a method of treating breast cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two hormone therapies independently selected from tamoxifen, Toremifene (Fareston), Fulvestrant (Faslodex), Megestrol acetate (Megace), ovarian ablation, Raloxifene, a luteinizing hormone-releasing hormone (LHRH) analogs (including goserelin and leuprolide), Megestrol acetate (Megace), and one or more aromatase inhibitors. In another embodiment, the invention is directed to a method of treating breast cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two hormone therapies and one of the hormone therapies is an aromatase inhibitors selected from letrozole (Femara), anastrozole (Arimidex), and exemestane (Aromasin). In another embodiment, the invention is directed to a method of treating breast cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two antibodies independently selected from ^(α)IGF-1R A12 MoAb, ^(α)IGF-1R 19D12 MoAb, ^(α)IGF-1R h7C10 MoAb, ^(α)IGF-1R CP-751871 MoAb, bevacizumab (Avastin), and trastuzumab.

In another embodiment, the invention is directed to a method of treating breast cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents and one of the chemotherapeutic agents is erlotinib.

In another embodiment, the invention is directed to a method of treating breast cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two of the chemotherapeutic agents and one or two of the chemotherapeutic agents are independently selected from rapamycin, lapatinib, erlotinib, N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof, N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof, N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof, and N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof.

In another embodiment, the invention is directed to a method of treating breast cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two of the antibodies. In another embodiment, the invention is directed to a method of treating breast cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two antibodies and one of the antibodies is trastuzumab.

In another embodiment, the invention is directed to a method of treating breast cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two of the chemotherapeutic agents and one of the chemotherapeutic agents is selected from N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, and N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine; optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof.

In another embodiment, the invention is directed to a method of treating breast cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two of the chemotherapeutic agents and one of the chemotherapeutic agents is N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta-[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof.

In another embodiment, the invention is directed to a method of treating non-small cell lung cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, radiation, one or more antibodies, and one or more chemotherapeutic agents. In another embodiment, the invention is directed to a method of treating non-small cell lung cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from cisplatin, oxaliplatin, carboplatin, Zactima (ZD6474), Paclitaxel, Docetaxel (Taxotere®), Gemcitabine (Gemzar®), Vinorelbine, Irinotecan, Etoposide, Vinblastine, Erlotinib (Tarceva®), gefitinib (Iressa), and Pemetrexed. In another embodiment, the invention is directed to a method of treating non-small cell lung cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is an antibody and the antibody is Bevacizumab. In another embodiment, the invention is directed to a method of treating non-small cell lung cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from cisplatin, oxaliplatin, carboplatin, Paclitaxel, Docetaxel (Taxotere®), and erlotinib (Tarceva®).

In another embodiment, the invention is directed to a method of treating non-small cell lung cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents and one of the chemotherapeutic agents is carboplatin.

In another embodiment, the invention is directed to a method of treating non-small cell lung cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents and one of the chemotherapeutic agents is selected from N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine, and N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclo-penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine; optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof. In another embodiment, the invention is directed to a method of treating non-small cell lung cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents and one of the chemotherapeutic agents is N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta-[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof.

In another embodiment, the invention is directed to a method of treating small cell lung cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, radiation, and one or two chemotherapeutic agents. In another embodiment, the invention is directed to a method of treating small cell lung cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapy agents independently selected from a platin (such as cisplatin, oxaliplatin, and carboplatin), gefitinib, vinorelbine, docetaxel, paclitaxel, etoposide, fosfamide, ifosfamide, cyclophosphamide, cyclophosphamide/doxorubicin/vincristine (CAV), doxorubicin, vincristine, gemcitabine, paclitaxel, vinorelbine, topotecan, irinotecan, methotrexate, and docetaxel.

In another embodiment, the invention is directed to a method of treating papillary or anaplastic thyroid cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, radiation, radioactive iodine therapy, one or two hormone therapies, and one or two chemotherapeutic agents. In another embodiment, the invention is directed to a method of treating papillary or anaplastic thyroid cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from thyroid hormone pills, Doxorubucin and a platin. In another embodiment, the invention is directed to a method of treating papillary or anaplastic thyroid cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is hormone therapy and the hormone therapy is radioiodine ablation.

In another embodiment, the invention is directed to a method of treating endometrial cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, radiation, one or two hormone therapies, and one or two chemotherapeutic agents. In another embodiment, the invention is directed to a method of treating endometrial cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two hormone therapies independently selected from megestrol acetate, Tamoxifen, and a progestin including medroxyprogesterone acetate (Provera) and megestrol acetate (Megace). In another embodiment, the invention is directed to a method of treating endometrial cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from a platinum-containing compound (including cisplatin, oxaliplatin, and carboplatin, more for example cisplatin), a taxane (including paclitaxel), doxorubicin (Adriamycin), cyclophosphamide, fluorouracil (5-FU), methotrexate, and vinblastine.

In another embodiment, the invention is directed to a method of treating ovarian cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, radiation, one or two antibodies, and one or two chemotherapeutic agents. In another embodiment, the invention is directed to a method of treating ovarian cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is an antibody and the antibody is bevacizumab. In another embodiment, the invention is directed to a method of treating ovarian cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from a platinum-containing compound (including cisplatin, oxaliplatin and carboplatin), a taxane (including paclitaxel and docetaxel), topotecan, an anthracyclines (including doxorubicin and liposomal doxorubicin), gemcitabine, cyclophosphamide, vinorelbine (Navelbine), hexamethylmelamine, ifosfamide, etoposide, bleomycin, vinblastine, ifosfamide, vincristine, and cyclophosphamide. In another embodiment, the invention is directed to a method of treating ovarian cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from a platin and a taxane. In another embodiment, the invention is directed to a method of treating ovarian cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from cisplatin, oxaliplatin, carboplatin, paclitaxel, and docetaxel.

In another embodiment, the invention is directed to a method of treating glioblastoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, radiation, one or two chemotherapeutic agents, one or two anti-seizure agents, and one or two agents to reduce swelling. In another embodiment, the invention is directed to a method of treating glioblastoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is radiation selected from external beam radiation, interstitial radiotherapy, and stereotactic radiosurgery. In another embodiment, the invention is directed to a method of treating glioblastoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from carmustine (BCNU), Erlotinib (Tarceva), bevacizumab, gefitinib (Iressa), rapamycin, temozolomide, cisplatin, BCNU, lomustine, procarbazine, and vincristine. In another embodiment, the invention is directed to a method of treating glioblastoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is an anti-seizure agent and the anti-seizure agent is diphenylhydantoin (Dilantin). In another embodiment, the invention is directed to a method of treating glioblastoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is an agents to reduce swelling and the agent is dexamethasone (Decadron). In another embodiment, the invention is directed to a method of treating glioblastoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents. In another embodiment, the invention is directed to a method of treating glioblastoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from erlotinib and temozolomide.

In another embodiment, the invention is directed to a method of treating cervical cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, radiation, and one or two chemotherapeutic agents. In another embodiment, the invention is directed to a method of treating cervical cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is surgery selected from cryosurgery, laser surgery, loop electrosurgical excision, conization, simple hysterectomy, and radical hysterectomy and pelvic lymph node dissection. In another embodiment, the invention is directed to a method of treating cervical cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is radiation selected from called external beam radiation therapy and brachytherapy. In another embodiment, the invention is directed to a method of treating cervical cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from a platinum compound (such as cisplatin, carboplatin, and oxaliplatin), paclitaxel, topotecan, ifosfamide, gemcitabine, vinorelbine, and fluorouracil.

In another embodiment, the invention is directed to a method of treating a gastrointestinal carcinoid tumor which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, radiation, immunotherapy, and one or two chemotherapeutic agents. In another embodiment, the invention is directed to a method of treating a gastrointestinal carcinoid tumor which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is surgery selected from excision and electrofulguration. In another embodiment, the invention is directed to a method of treating a gastrointestinal carcinoid tumor which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from cyproheptadine, SOM230, octreotide and lanreotide. In another embodiment, the invention is directed to a method of treating a gastrointestinal carcinoid tumor which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is immunotherapy and the immunotherapy is an interferon.

In another embodiment, the invention is directed to a method of treating a gastrointestinal stromal tumor which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, radiation, and one or two chemotherapeutic agents. In another embodiment, the invention is directed to a method of treating a gastrointestinal stromal tumor which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from imatinib mesylate (Gleevec), sunitinib (Sutent), and nilotinib (AMN107).

In another embodiment, the invention is directed to a method of treating hepatocellular carcinoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from surgery, radiofrequency ablation, ethanol ablation, cryosurgery, hepatic artery embolization, chemoembolization, radiation, and one or two chemotherapeutic agents. In another embodiment, the invention is directed to a method of treating hepatocellular carcinoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is surgery selected from resection and transplantation. In another embodiment, the invention is directed to a method of treating hepatocellular carcinoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents independently selected from sorafenib, 5-fluorouracil and cisplatin.

In another embodiment, the invention is directed to a method of treating non-Hodgkin's lymphoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments independently selected from radiation, one or two chemotherapeutic agents, interferon therapy, one or two antibodies, and bone marrow or peripheral blood stem cell transplantation. In another embodiment, the invention is directed to a method of treating non-Hodgkin's lymphoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is one or two chemotherapeutic agents selected from CHOP (cyclophosphamide, doxorubicin, vincristine and prednisone), chlorambucil, fludarabine, and etoposide. In another embodiment, the invention is directed to a method of treating non-Hodgkin's lymphoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is an antibody selected from rituximab, ibritumomab tiuxetan, tositumomab, and alemtuzumab. In another embodiment, the invention is directed to a method of treating non-Hodgkin's lymphoma which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is an antibody and the anitbody is rituximab.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is radiation and another treatment is surgery.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is radiation and another treatment is one or two chemotherapeutic agents.

In another embodiment, the invention is directed to a method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a Compound of Formula I, as defined in the Summary of the Invention, in combination with one or more treatments where one of the treatments is surgery and another treatment is one or two chemotherapeutic agents.

For each of the foregoing embodiments, the Compound of Formula I is selected from any of the following embodiments, including from the Representative Compounds in Table 1.

One embodiment (A) of the invention is directed to a compound of Formula I where W¹, W², W³, and W⁴ are —C(R¹)═; or one or two of W¹, W², W³, and W⁴ are independently —N═ and the remaining are —C(R¹)═; where each R¹ is independently hydrogen, alkyl, haloalkyl, nitro, alkoxy, haloalkoxy, halo, hydroxy, cyano, amino, alkylamino, or dialkylamino; and all other groups are as defined in the Summary of the Invention. In another embodiment, W¹, W², W³, and W⁴ are —C(R¹)═ and each R¹ is independently hydrogen or alkyl; or one of W¹ and W⁴ is —N═ and the other is —C(H)═. In another embodiment, W¹, W², W³, and W⁴ are —C(R¹)═ where each R¹ is independently hydrogen or alkyl. In another embodiment, R¹ is hydrogen.

Another embodiment (B) of the invention is a Compound of Formula I where R⁵⁰ is hydrogen, alkyl, alkenyl, halo, haloalkyl, haloalkenyl, hydroxy, alkoxy, alkenyloxy, haloalkoxy, nitro, amino, alkylamino, dialkylamino, —N(R⁵⁵)C(O)—C₁-C₆-alkylene-N(R^(55a))R^(55b), alkylcarbonyl, alkenylcarbonyl, carboxy, alkoxycarbonyl, cyano, alkylthio, —S(O)₂NR⁵⁵R^(55a), or alkylcarbonylamino; where R⁵⁵ and R^(55b) are independently hydrogen, alkyl, or alkenyl and R^(55a) is hydrogen, alkyl, alkenyl, hydroxy, or alkoxy; and all other groups are as defined in the Summary of the Invention. In another embodiment, R⁵⁰ is hydrogen.

Another embodiment (C) of the invention is a Compound of Formula I where R⁵¹ is hydrogen or alkyl; and all other groups are as defined in the Summary of the Invention. In another embodiment, R⁵¹ is alkyl. In another embodiment, R⁵¹ is methyl.

Another embodiment (D) of the invention is a Compound of Formula I where R⁵² is hydrogen or halo; and all other groups are as defined in the Summary of the Invention. In another embodiment R⁵² is hydrogen or fluoro. In another embodiment, R⁵² is hydrogen.

Another embodiment (E) of the invention is a Compound of Formula I where R⁵³ is hydrogen, alkyl, alkenyl, halo, haloalkyl, haloalkenyl, hydroxy, alkoxy, alkenyloxy, haloalkoxy, nitro, amino, alkylamino, dialkylamino, —N(R⁵⁵)C(O)—C₁-C₆-alkylene-N(R^(55a))R^(55b), alkylcarbonyl, alkenylcarbonyl, carboxy, alkoxycarbonyl, cyano, alkylthio, —S(O)₂NR⁵⁵R^(55a), or alkylcarbonylamino; where R⁵⁵ and R^(55b) are independently hydrogen, alkyl, or alkenyl and R^(55a) is hydrogen, alkyl, alkenyl, hydroxy, or alkoxy; and all other groups are as defined in the Summary of the Invention. In another embodiment, R⁵³ is hydrogen, alkoxy, nitro, amino, or —N(R⁵⁵)C(O)—C₁-C₆-alkylene-N(R^(55a))R^(55b). In another embodiment, R⁵³ is hydrogen, methoxy, nitro, amino, or —NHC(O)CH₂N(CH₃)₂. In another embodiment, R⁵³ is hydrogen or methoxy.

Another embodiment (F) of the invention is a Compound of Formula I where R⁵⁴ is hydrogen, alkyl, alkenyl, halo, haloalkyl, haloalkenyl, hydroxy, alkoxy, alkenyloxy, haloalkoxy, nitro, amino, alkylamino, dialkylamino, —N(R⁵⁵)C(O)—C₁-C₆-alkylene-N(R^(55a))R^(55b), alkylcarbonyl, alkenylcarbonyl, carboxy, alkoxycarbonyl, cyano, alkylthio, —S(O)₂NR⁵⁵R^(55a), or alkylcarbonylamino; where R⁵⁵ and R^(55″) are independently hydrogen, alkyl, or alkenyl and R^(55a) is hydrogen, alkyl, alkenyl, hydroxy, or alkoxy; and all other groups are as defined in the Summary of the Invention. In another embodiment, R⁵⁴ is hydrogen, alkyl, alkoxy, or halo. In another embodiment, R⁵⁴ is hydrogen, methyl, methoxy, bromo, or chloro. In another embodiment, R⁵⁴ is hydrogen, methoxy, or chloro.

Another embodiment (G) of the invention is directed to a compound of Formula I where R⁵⁰, R⁵², and R⁵³ are hydrogen and R⁵⁴ is halo or alkoxy; R⁵⁰, R⁵², and R⁵⁴ are hydrogen and R⁵³ is alkoxy; or R⁵⁰ and R⁵² are hydrogen and R⁵³ and R⁵⁴ together with the carbons to which they are attached form a 6-membered heteroaryl; and all other groups are as defined in the Summary of the Invention. In another embodiment, R⁵⁰, R⁵², and R⁵³ are hydrogen and R⁵⁴ is chloro or methoxy; R⁵⁰, R⁵², and R⁵⁴ are hydrogen and R⁵³ is methoxy; or R⁵⁰ and R⁵² are hydrogen and R⁵³ and R⁵⁴ together with the carbons to which they are attached form pyridinyl. Even more specifically, R⁵⁰, R⁵², and R⁵³ are hydrogen and R⁵⁴ is chloro or methoxy; or R⁵⁰, R⁵², and R⁵⁴ are hydrogen and R⁵³ is methoxy.

In another embodiment (G1) of embodiment G is a compound of Formula I where R⁵¹ is methyl.

Another embodiment (H) of the invention is a compound of Formula I where B is phenyl substituted with R^(3a) and optionally further substituted with one, two, or three R³; and all other groups are as defined in the Summary of the Invention. In another embodiment, B is phenyl substituted with R^(3a). In another embodiment the Compound is of Formula I(a):

In another embodiment, B is phenyl substituted with R^(3a) as depicted in Ia and is not further substituted with R³.

Another embodiment of the Invention (J) is directed to a compound of Formula I where B is heteroaryl optionally substituted with one, two, or three R³. In another embodiment, B is thien-3-yl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, oxazolyl, isoxazolyl, pyrrolyl, imidazolyl, pyrazolyl, or thiazolyl, each of which is optionally substituted with one or two R³. In another embodiment, B is thien-3-yl, pyridin-2-yl, pyridin-3-yl, pyridin-4-yl, oxazol-2-yl, oxazol-4-yl, oxazol-5-yl, isoxazol-3-yl, isoxazol-4-yl, isoxazol-5-yl, imidazol-2-yl, pyrrol-2-yl, pyrrol-3-yl, imidazol-4-yl, imidazol-5-yl, pyrazol-3-yl, pyrazol-4-yl, or pyrazol-5-yl, each of which is optionally substituted with one or two R³. In another embodiment, B is thien-3-yl, pyridin-3-yl, pyridin-4-yl, isoxazol-4-yl, or pyrazol-4-yl, each of which is optionally substituted with one or two R³. In another embodiment, B is pyridin-3-yl, 2-hydroxy-pyridin-5-yl, isoxazol-4-yl, or pyrazol-4-yl, each of which is optionally substituted with one or two R³.

Another embodiment (K) provides a compound of Formula I or Ia where R^(3a) is cyano; hydroxyamino; carboxy; alkylsulfonyl, aminoalkyloxy; alkylaminoalkyloxy; dialkylaminoalkyloxy; —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)); —C(O)NR⁸R^(8a); —NR⁹C(O)R^(9a); —C(O)N(R¹⁰—C₁-C₆-alkylene-N(R^(10a))R^(10b); —NR¹¹C(O)NR^(11a)R^(11b) where R^(11a); —C(O)R¹²; —NR¹³C(O)OR^(13a); —C(O)N(R¹⁴)N(R^(14a))(R^(14b)); —S(O)₂N(R¹⁵)—C₁-C₆-alkylene-N(R^(15a))R^(15b); —C(O)N(R¹⁶)—C₁-C₆-alkylene-C(O)OR^(16a); heteroaryl optionally substituted with one or two aminoalkyl, alkylaminoalkyl, or dialkylaminoalkyl; —N(R¹⁷)— C(═N(R^(17b))(R^(17a)))(NR^(17c)R^(17d)); —N(R¹⁸)C(O)—C₁-C₆-alkylene-N(R^(18b))C(O)R^(18a); —C(O)N(R¹⁹)—C₁-C₆-alkylene-C(O)R^(19a); —N(R²²)C(O)—C₁-C₆-alkylene-N(R^(22b))—N(R^(22c))(R^(22a)); —C₀-C₆-alkylene-N(R²³)—C₁-C₆-alkylene-N(R^(23b))R^(23a); or —NR²⁴C(O)—C₁₋C₆-alkylene-OR^(24a); where each of the alkylene in R^(3a) is independently optionally further substituted with 1, 2, 3, 4, or 5 groups selected from halo, hydroxy, amino, alkylamino, and dialkylamino; and all other groups are as defined in the Summary of the Invention.

In another embodiment, R^(3a) is —NHC(O)CH₂NH(CH₃), —NHC(O)CH₂NH(CH₂CH₃), —NHC(O)CH(CH₃)NH₂, —NHC(O)C(CH₃)₂NH₂, —NHC(O)CH₂N(CH₃)₂, —NHC(O)CH₂N(CH₃)CH₂CH₂N(CH₃)₂, —NHC (O)CH(NH₂)CH₂CH₃, —NHC(O)CH₂N(CH₃)CH₂CH₂N(CH₃)₂, —NHC(O)CH(CH₃)NH(CH₃), —NHC(O)CH₂NH₂, —NHC(O)H, —NHC(O)CH₂(azetidin-1-yl), —NHC(O)(pyrrolidin-2-yl), —NHC(O)CH(NH₂)CH₂OH, —NHC(O)(azetidin-4-yl), —NHC(O)C(CH₃)₂NH(CH₃), —NH₂, —NHC(O)CH₂NH(CH₂CH₂CH₃), —NHC(O)CH₂CH₂NH₂, —NHOH, —NHC(O)(piperidin-3-yl), —NHC(O)CH₂(4-methyl-1,4-diazepan-1-yl), —NHC(O)CH(NH₂)(CH₂CH₃), —NHC(O)CH₂NH(CH₂CH(OH)(CH₃)), —NHC(O)CH₂NHCH₂CH₂F, —NHC(O)CH₂NH(OCH₂CH(CH₃)₂), —NHC(O)(1-aminocycloprop-1-yl), —NHC(O)CH₂NH(CH₂cyclopropyl), —NHC(O)CH₂(3-(dimethylamino)-azetidin-1-yl), —NHC(O)(piperidin-2-yl), —NHC(O)(morpholin-4-yl), —NHC(O)CH₂(pyrrolidin-1-yl), —NHC(O)CH(NH₂)CH₂CH₂CH₂CH₂N(CH₃)₂, —NHC(O)CH₂N(CH₃)(CH₂CH₃), —NHC(O)CH₂(imidazol-5-yl), —NHC(O)(1-aminocyclopent-1-yl), —NHC(O)CH₂NH(CH₂CH(CH₃)₂), —NHC(O)CH₂N(CH₃)(CH₂CH₃), —NHC(O)(N-(imidazol-4-ylmethyl)-azetidin-3-yl), —NHC(O)(N-ethyl-azetidin-3-yl), —NHCH₂N(CH₃)CH₂CH₂N(CH₃)₂, —NHC(O)CH₂N(CH₃)(N-methyl-pyrrolidin-3-yl), —NHC(O)CH₂N(CH₃)(CH₂CH₂N(CH₃)₂), —NHC(O)CH₂(3-hydroxy-pyrrolidin-1-yl), —NHC(O)(1-amino-cyclobut-1-yl), —NHC(O)CH₂NH(CH₂)₃CH₃, —NHC(O)CH₂(3-piperidin-1-ylazetidin-1yl), —NHC(O)NH₂, —NHC(O)(1-hydroxycyclopropyl), —NHC(O)CH₂NHN(CH₃)₂, —NHC(O)NH(CH₂)₂N(CH₃)₂, —NHC(O)CH₂OH, —NHC(O)(pyridazin-4-yl), —NHC(O)(N-methyl-piperidin-4-yl), —NHC(O)CH₂NHCH(CH₃)₃, —NHC(O)CH₂(3-dimethylamino-pyrrolidin-1yl), —NHC(O)CH₂NH(CH₂)₂N(CH₃)₂, —NHC(O)(1-cyclopropylmethyl-azetidin-3-yl), —NHC(O)CH₂NH(CH₃)₃, —NHC(O)(imidazol-2-yl), —NHC(O)(imidazol-4-yl), —NHC(O)(1,2-oxazol-5-yl), —NHC(O)CH₂NHCH₂CF₃, —NHC(O)CH₂CH₂(piperidin-1-yl), —NHC(O)(3-oxo-cyclopent-1-yl), —NHC(O)(2-hydroxy-pyridin-6-yl), —NHC(O)CH₂NH(3-fluoro-4-hydroxyphenyl), —NHC(O)(CH₂)₃N(CH₃)₂, —NHC(O)(1-(furan-2-ylmethyl)-azetidin-3-yl), —NHC(O)(pyrimidin-5-yl), —NHC(O)(pyrrol-2-yl), —NHC(O)CH₂N(CH₃)CH(CH₃)₂, —NHC(O)CH₂N(CH₂CH₃)₂, —NHC(O)CH₂(3-methyl-1,2-oxazol-5-yl), —NHC(O)CH₂NHCH₂(3-hydroxyphenyl), —NHC(O)(N-methyl-pyrrol-2-yl), —NHC(O)(2-amino-tetrahydropyran-2-yl), —NHC(O)CH₂(4-methylamino-piperidin-1-yl), —NHC(O)(piperidin-1-yl), —NHC(O)(N-methyl-pyrrolidin-2-yl), —NHC(O)(thien-3-yl), —NHC(O)(N-(cyclopropylcarbonyl)azetidin-3-yl), —NHC(O)CH₂(4-methylpiperazin-1-yl), —NHC(O)(N-benzylazetidin-3-yl), —NHC(O)(2-chloro-pyridin-3-yl), —NHC(O)CH₂(Pyridin-4-yl), —NHC(O)CH₂N(CH₃)(CH₂CH═CH₂), —NHC(O)CH₂NH(benzyl), —NHC(O)CH₂OCH₃, —NHC(O)[1-(C(O)CH₂CH₃)-azetidin-3-yl], —NHC(O)(pyridin-3-yl), —NHC(O)CH₂NHCH₂CH₂OCH₃, —NHC(O)(1-[C(O)CH₃]piperidin-4-yl), —NHC(O)CH₂(2-methyl-pyrrolidin-1-yl), —NHC(O)(furan-3-yl), —NHC(O)CH₂N(CH₃)₂, —NHC(O)(2-chloro-pyridin-5-yl), —NHC(O)(2-chlorophenyl), —NHC(O)CH₂(pyridin-2-yl), —NHC(O)CH₂(3-dimethylamino-azetidin-1-yl), —NHC(O)CH₂(pyridin-3-yl), —NHC(O)CH₂(2-chlorophenyl), —NHC(O)CH₂N(CH₃)CH₂CH₂CH₂N(CH₃)₂, —NHC(O)CH₂N(CH₂CH₃)CH₂CH₂OH, —NHC(O)CH₂(2-benzyl-pyrrolidin-1-yl), —NHC(O)(furan-2-yl, —NHC(O)(2-chloro-pyridin-4-yl), —NHC(O)CH₂NHC(O)CH₃, —NHC(O)CH₂CH₂CH₃, —NHC(O)(4-chlorophenyl), —NHC(O)(4-methyl-phenyl), —NHC(O)CH₂NHC(O)O(CH₃)₃, —NHC(O)(benzo[d][1,3]dioxol-5-yl), —NHC(O)CH₂NHOCH₂(2-methoxyphenyl), —NHC(O)(pyridin-4-yl), —NHC(O)CH_(2[)4-(3,4-dichlorophenyl)-piperazin-1-yl], —NHC(O)CH₂CH₂(pyridin-3-yl), —NHC(O)(tetrahydrofuran-3-yl), —NHC(O)CH₂NHCH₂(2-methylphenyl), —NHC(O)CH(CH₃)CH₂CH₃, —NHC(O)CH₂(3-fluorophenyl), —NHC(O)CH₂C(CH₃)₂phenyl, —NHC(O)(2-methyl-cycloprop-1-yl), —NHC(O)(2-methyl-4-methoxyphenyl), —NHC(O)(2-methylpyridin-3-yl), —NHC(O)(4-methoxyphenyl), —NHC(O)CH₂(4-ethylpiperazin-1-yl), —NHC(O)(thien-2-yl), —NHC(O)(3-fluoro-2-methylphenyl), —NHC(O)(2-bromo-thien-3-yl), —NHC(O)(4-fluorophenyl), —NHC(O)CH₂(3-methylpiperidin-1-yl), —NHC(O)CH(CH₃)₂, —NHC(O)(CH₂)₃CH₃, —NHC(O)CH₂OCH₂CH₃, —NHC(O)CH₂NH(2-fluorophenyl), —NHC(O)(3-dimethylaminophenyl), —NHC(O)CH₂(4-methylpiperidin-1-yl), —NHC(O)CH₂NH(2-n-propylphenyl), —NHC(O)phenyl, —NHC(O)(pyrazin2-yl), —NHC(O)(3-fluoro-4-methoxyphenyl), —NHC(O)C(CH₃)₂CH₂CH₃, —NHC(O)CH₂O(4-fluorophenyl), —NHC(O)(1-methylcarbonyl-azetidin-3-yl), —NHC(O)CH₂NH(4-methylphenyl), —NHC(O)CH₂NH(phenyl), —NHC(O)CH₂(4-allyl-piperazin-1-yl), —NHC(O)(2-methylphenyl), —NHC(O)CH₂CH₂OCH₃, —NHC(O)(3-methyl-furan-2-yl), —NHC(O)C(CH₃)₃, —NHC(O)CH₂NHObenzyl, —NHC(O)CH₂NH(3-chlorophenyl), —NHC(O)cyclobutyl, —NHC(O)CH₂(3-methoxyphenyl), —NHC(O)(1-methylcycloprop-1-yl), —NHC(O)(3-fluorophenyl), —NHC(O)(4-dimethylaminophenyl), —NHC(O)(3,4-dichlorophenyl), —NHC(O)CH₂NHCH₂(2-methylthiophenyl), —NHC(O)CH₂(2-fluorophenyl), —NHC(O)CH₂N(CH₂CH₃)CH(CH₃)₂, —NHC(O)(thiazol-4-yl), —NHC(O)CH₂N(CH₃)benzyl, —NHC(O)CH₂NHCH₂(thien-2-yl), —NHC(O)CH₂NHCH₂(pyridin-2-yl), —NHC(O)(3-methoxyphenyl), —NHC(O)CH₂NHCH₂(3-chloro-4-methylphenyl), —NHC(O)CH(CH₃)CH₂CH₂CH₃, —NHC(O)CH₂(4-chlorophenyl), —NHC(O)(3-fluoro-4-methylphenyl), —NHC(O)CH₂O(2-methylphenyl), —NHC(O)CH₂(cyclohexyl), —NHC(O)(2-phenyl-cycloprop-1-yl), —NHC(O)(3-chlorophenyl), —NHC(O)CH₂(2-methoxyphenyl), —NHC(O)CH₂CH₂(3-methoxyphenyl), —NHC(O)CH₂NH(2-fluoro-4-methyl-phenyl), —NHC(O)CH₂NHCH₂(3-fluoro-phenyl), —NHC(O)CH₂(4-methoxy-phenyl), —NHC(O)benzyl, —NHC(O)(2,4-dichlorophenyl), —NHC(O)(3-oxo-cyclohex-1-yl), —NHC(O)CH₂NH(3-fluorophenyl), —NHC(O)CH₂(3-chlorophenyl), —NHC(O)CH₂NHCH₂CH(CH₃)phenyl, —NHC(O)CH₂NHCH₂(2,4-dimethylphenyl), —NHC(O)CH₂(2-methyl-piperidin-1-yl), —NHC(O)CH₂NH(2-methoxyphenyl), —NHC(O)CH₂(1,2,3,4-tetrahydroisoquinolin-2-yl), —NHC(O)CH₂CH₂CH═CH₂, —NHC(O)CH₂NH(2-methylphenyl), —NHC(O)CH₂(4-oxo-piperidin-1-yl), —NHC(O)(2-fluorophenyl), —NHC(O)CH₂NHCH(CH₃)phenyl, —NHC(O)(2-fluoro-6-methoxyphenyl), —NHC(O)CH₂NH(2-isopropylphenyl), —NHC(O)CH₂CH₂(2-methoxyphenyl), —NHC(O)CH₂CH₂CH(CH₃)₂, —NHC(O)CH₂(2-phenyl-morpholin-4-yl), —NHC(O)CH₂CH₂(4-methoxyphenyl), —NHC(O)CH₂N(allyl)cyclopentyl, —NHC(O)CH₂N(CH₃)CH₂CH₂OCH₃, —NHC(O)CH₂CH₂C(O)cyclopropyl, —NHC(O)CH₂NH(3-tert-butylphenyl), —NHC(O)CH₂N(n-propyl)(cyclopropylmethyl), —NHC(O)CH₂(2-oxo-cyclopentyl), —NHC(O)CH₂NH(4-chlorophenyl), —NHC(O)CH₂(4-piperidin-1-ylpiperidin-1-yl), —NHC(O)CH₂(4-cyclopentylpiperazin-1-yl), —NHC(O)CH₂(2-methylphenyl), —NHC(O)CH₂NHCH₂(3-fluoro-6-methylphenyl), —NHC(O)CH₂C(CH₃)₃, —NHC(O)CH₂NH(2-chlorophenyl), —NHC(O)(3-fluoro-6-methylphenyl), —NHC(O)(4-fluoro-3-methylphenyl), —NHC(O)(2,3-dichlorophenyl), —NHC(O)CH₂O phenyl, —NHC(O)CH₂NH(2,3-dimethylphenyl), —NHC(O)(2-fluoro-5-methylphenyl), —NHC(O)CH₂NHOCH₂(4-methylphenyl), —NHC(O)CH₂(4-isopropylpiperazin-1-yl), —NHC(O)CH₂(4-fluorophenyl), —NHC(O)CH₂CH(CH₃)₂, —NHC(O)(2-methoxy-4-methylphenyl), —NHC(O)CH₂(4-n-propylpiperidin-1-yl), —NHC(O)CH₂O(3-methylphenyl), —NHC(O)(tetrahydrofuran-2-yl), —NHC(O)CH₂(3-hydroxymethylpiperidin-1-yl), —NHC(O)(1-tert-butoxycarbonylpiperidin-2-yl), —NHC(O)CH₂N(CH₃)CH₂(pyridin-3-yl), —NHC(O)CH₂N(CH₂CH₃)phenyl, —NHC(O)CH₂OCH₂CH₂OCH₃, —NHC(O)CH₂CH₂(cyclopentyl), —NHC(O)(2,5-dichlorophenyl), —NHC(O)CH₂(4-methylcarbonylpiperazin-1-yl), —NHC(O)(5-fluoro-2-methoxyphenyl), —NHC(O)CH₂N(CH₂CH₃)cyclohexyl, —NHC(O)(5-methyl-1,2-oxazol-3-yl), —NHC(O)(3-methylpyridin-3-yl), —NHC(O)(2-methoxypyridin-3-yl), —NHC(O)(3,5-dichlorophenyl), —NHC(O)CH₂(thiazolidin3-yl), —NHC(O)CH₂(4-[C(O)H]-piperazin-1-yl), —NHC(O)CH₂(2-pyridin-4-ylpiperidin-1-yl), —NHC(O)(2-methoxyphenyl), —NHC(O)CH₂N(CH₃)CH₂CH(CH₃)₂, —NHC(O)CH₂(4-[C(O)H]-homopiperazin-1-yl), —NHC(O)(1-phenylcycloprop-1-yl), —NHC(O)CH₂(2,6-dimethylmorpholin-4-yl), NHC(O)CH₂(2-phenylpyrrolidin-1-yl), —NHC(O)CH₂(morpholin-4-yl), —C(O)NHCH(CH₃)CH₂N(CH₃)₂, —C(O)NHCH₂CH₂N(CH₃)₂, —C(O)NH(pyrrolidin-3-yl), —C(O)NHCH₂CH₂(pyrrolidin-1-yl), —C(O)NHCH₂CH₂NH₂, —C(O)N(CH₃)CH₂CH₂N(CH₃)₂, —C(O)NHCH₂(piperidin-2-yl), —C(O)NH(1-methylazetidin-3-yl), —C(O)NHCH₂CH₂(piperidin-1-yl), —C(O)NHCH₂CH₂N(CH₂CH₃)₂, —C(O)NH(1-methylpiperidin-3-yl), —C(O)NH(piperidin-3-yl), —C(O)NHCH₂(1-methylpiperidin-3-yl), —C(O)NHCH₂CH₂N(CH₂CH₂OH)₂, —C(O)NH(1-ethylpiperidin-3-yl), —C(O)NH₂, —C(O)(3-aminopyrrolidin-1-yl), —C(O)(3-methylaminopyrrolidin-1-yl), —C(O)OH, —C(O)NHCH₂CH₂(morpholin-4-yl), —C(O)NHCH₂(1-ethylpyrrolidin-2-yl), —C(O)(4-amino-3-oxo-pyrazolidin-1-yl), —C(O)NHCH₃, —C(O)(3-aminocyclobut-1-yl), —C(O)NHCH₂(pyridin-3-yl), —C(O)NHCH₂CH₂OH, —C(O)NH(3-oxo-pyrazolidin-4-yl), —NHCH₂CH₂(imidazol-4-yl), —C(O)(3-dimethylaminopyrrolidin-1-yl), —C(O)NHCH₂(pyridin-4-yl), —C(O)N(CH₃)(1-methyl-pyrrolidin-3-yl), —C(O)(3-diethylaminopyrrolidin-1-yl), —C(O)NH(pyrrol-1-yl), —C(O)NHCH₂CH₂CH₂(pyrrolidin-1-yl), —C(O)N(CH₃)CH₂CH₂CN, —C(O)NHCH₂CH₂OCH₃, —C(O)N(CH₂CH₃)CH₂CH₂CN, —C(O)(3-aminopiperidin-1-yl), —C(O)NHCH₂CH₂CH₂N(CH₃)₂, —C(O)NH(morpholin-4-yl), —C(O)NHN(CH₃)₂, —C(O)NHCH₂CH₂CH₂(imidazol-1-yl), —C(O)NHCH₂CH₂CH₂N(CH₂CH₃)₂, —C(O)NHCH₂CH₂CN, —C(O)NHCH₂CH₂C(O)OCH₃, —C(O)NHCH₂CH₂SCH₃, —C(O)NHCH₂CH₂SCH₂CH₃, —C(O)N(CH₂CH₃)CH₂CH₂N(CH₃)₂, —C(O)NHCH₂CH₂CH₂(2-oxo-pyrrolidin-1-yl), —C(O)NHCH₂CH₂(pyridin-4-yl), —C(O)NHCH₂CH₂CH₂OCH₂CH₃, —C(O)NHCH₂CH₂CH₂(morpholin-4-yl), —C(O)NHCH₂CH₂CH₂OCH₃, —C(O)N(CH₃)CH₂CH₂CH₂N(CH₃)₂, —C(O)NHCH₂CH₂CH₂OCH₂CH₂CH₃, —C(O)NHCH₂CH₂C(O)OCH₂CH₃, —C(O)NHCH₂CH₂CH₂OCH(CH₃)₂, —C(O)NHC(CH₃)₂CH₂(piperidin-1-yl), —C(O)N(CH₃)CH₂CH₂CH₃, —C(O)NH(piperidin-1-yl), —C(O)NHCH(CH₃)CH₂OCH₃, —C(O)NHC(CH₃)₂CH₂(morpholin-4-yl), —C(O)(2-dimethylaminomethylpiperidin-1-yl), —C(O)NH(CH₂)₃—O—(CH₂)₃CH₃, —C(O)NHCH(CH₃)(CH₂)₃N(CH₂CH₃)₂, —C(O)NHC(CH₃)₂C(O)(piperidin-1-yl), —C(O)(4-methylpiperazin-1-yl), —C(O)(2-piperidin-1-ylmethyl-piperidin-1-yl), cyano, —NHCH₃, —CH(CH₃)NHCH₂CH₂N(CH₃)₂, —C(O)CH₃, —S(O)₂NHCH₂CH₂N(CH₃)₂, —S(O)₂NH(CH₂)₃N(CH₃)₂, 5-(N,N-dimethylaminomethyl)-1,3,4-oxadiazol-2-yl, —NHCH₂CH₂N(CH₃)₂, —N(CH₃)₂, —OCH₂CH₂N(CH₃)₂, —NHC[N(CH₃)₂][═N(CH₃)₂], —OCH F₂, —S(O)₂CH₃, —OCF₃, or —NHC(O)CH₂(4-dimethylaminopiperidin-1-yl).

In another embodiment (L), the compound of Formula I or Ia is that where R^(1a) is hydroxyamino, —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)), —C(O)NR⁸R^(8a), —NR⁹C(O)R^(9a), —C(O)N(R¹⁰—C₁-C₆-alkylene-N(R^(10a))R^(10b), —NR¹¹C(O)NR^(11a)R^(11b), —N(R²²)C(O)—C₁-C₆-alkyene-N(R^(22b))—N(R^(22c))(R^(22a)), —NR¹³C(O)OR^(13a), —N(R¹⁸)C(O)—C₁-C₆-alkylene-N(R^(18b))C(O)R^(18a), —NR²⁴C(O)—C₁₋C₆-alkylene-OR^(24a), or —N(R²⁰)C(O)—C₁-C₆-alkylene-C(O)R^(20a); where each of the alkylene in R^(3a) is independently optionally further substituted with 1, 2, 3, 4, or 5 groups selected from halo, hydroxy, and amino; and all other groups are as defined in the Summary of the Invention. In another embodiment, R^(3a) is —NHC(O)CH₂NH(CH₃), —NHC(O)CH(CH₃)NH₂, —NHC(O)C(CH₃)₂NH₂, —NHC(O)CH₂N(C H₃)₂, —NHC(O)CH₂N(CH₃)CH₂CH₂N(CH₃)₂, —NHC(O)CH(NH₂)CH₂CH₃, —NHC(O)CH₂N(C H₃)CH₂CH₂N(CH₃)₂, —NHC(O)CH(CH₃)NH(CH₃), —NHC(O)H, —NHC(O)CH₂(azetidin-1-yl), —NHC(O)(pyrrolidin-2-yl), —NHC(O)CH(NH₂)CH₂OH, —NHC(O)(azetidin-4-yl), —NHC(O)C(CH₃)₂NH(CH₃), —NH₂, —NHC(O)CH₂NH(CH₂CH₂CH₃), —NHC(O)CH₂CH₂NH₂, —NHOH, or —NHC(O)(piperidin-3-yl).

In another embodiment (M) the compound is of Formula I or Ia and R^(3a)—N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)); and R⁷ is hydrogen or alkyl and R^(7a) and R^(7b) are independently hydrogen, alkyl, aminoalkyl, alkylaminoalkyl, or dialkylaminoalkyl; and all other groups are as defined in the Summary of the Invention. In another embodiment, R^(3a) is —NHC(O)CH₂NH(CH₃), —NHC(O)CH(CH₃)NH₂, —NHC(O)C(CH₃)₂NH₂, —NHC(O)CH₂N(CH₃)₂, —NHC(O)CH₂N(CH₃)CH₂CH₂N(CH₃)₂, —NHC(O)CH(NH₂)CH₂CH₃, —NHC(O)CH₂N(CH₃)CH₂CH₂N(CH₃)₂, or —NHC(O)CH(CH₃)NH(CH₃).

Embodiment (N) provides a compound of Formula I where each R³ is independently halo; cyano; alkyl; alkenyl; alkoxy; hydroxyamino; carboxy; alkylsulfonyl, aminoalkyloxy; alkylaminoalkyloxy; dialkylaminoalkyloxy; —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)); —C(O)NR⁸R^(8a); —NR⁹C(O)R^(9a); —C(O)N(R¹⁰)—C₁-C₆-alkylene-N(R^(10a))R^(10b); —(NR¹¹C(O)NR^(11a)R^(11b) where R^(11a); —C(O)R¹²; —NR¹³C(O)OR^(13a); —C(O)N(R¹⁴)N(R^(14a))(R^(14b)); —S(O)₂N(R¹⁵)—C₁-C₆-alkylene-N(R^(15a))R^(15b); —C(O)N(R¹⁶)—C₁-C₆-alkylene-C(O)OR^(16a); heteroaryl optionally substituted with one or two aminoalkyl, alkylaminoalkyl, or dialkylaminoalkyl; —N(R¹⁷)—C(═N(R^(17b))(R^(17a)))(NR^(17c))(R^(17d)); —N(R¹⁸)C(O)—C₁-C₆-alkylene-N(R^(18b))C(O)R^(18a); —C(O)N(R¹⁹)—C₁-C₆-alkylene-C(O)R^(19a); —N(R²²)C(O)—C₁-C₆-alkylene-N(R^(22b))—N(R^(22c))(R^(22a)); —C₀-C₆-alkylene-N(R²³)—C₁-C₆-alkylene-N(R^(23b))R^(23a); or —NR²⁴C(O)—C₁-C₆-alkylene-OR^(24a); where each of the alkylene in R³ is independently optionally further substituted with 1, 2, 3, 4, or 5 groups selected from halo, hydroxy, amino, alkylamino, and dialkylamino; and all other groups are as defined in the Summary of the Invention.

In another embodiment, each R³ is independently methyl, bromo, chloro, fluoro, —NHC(O)CH₂NH(CH₃), —NHC(O)CH₂NH(CH₂CH₃), —NHC(O)CH(CH₃)NH₂, —NHC(O)C(CH₃)₂NH₂, —NHC(O)CH₂N(CH₃)₂, —NHC(O)CH₂N(CH₃)CH₂CH₂N(CH₃)₂, —NHC(O)CH(NH₂)CH₂CH₃, —NHC(O)CH₂N(CH₃)CH₂CH₂N(CH₃)₂, —NHC(O)CH(CH₃)NH(CH₃), —NHC(O)CH₂NH₂, —NHC(O)H, —NHC(O)CH₂(azetidin-1-yl), —NHC(O)(pyrrolidin-2-yl), —NHC(O)CH(NH₂)CH₂OH, —NHC(O)(azetidin-4-yl), —NHC(O)C(CH₃)₂NH(CH₃), —NH₂, —NHC(O)CH₂NH(CH₂CH₂CH₃), —NHC(O)CH₂CH₂NH₂, —NHOH, —NHC(O)(piperidin-3-yl), —NHC(O)CH₂(4-methyl-1,4-diazepan-1-yl), —NHC(O)CH(NH₂)(CH₂CH₃), —NHC(O)CH₂NH(CH₂CH(OH)(CH₃)), —NHC(O)CH₂NHCH₂CH₂F, —NHC(O)CH₂NH(OCH₂CH(CH₃)₂), —NHC(O)(1-aminocycloprop-1-yl), —NHC(O)CH₂NH(CH₂cyclopropyl), —NHC(O)CH₂(3-(dimethylamino)-azetidin-1-yl), —NHC(O)(piperidin-2-yl), —NHC(O)(morpholin-4-yl), —NHC(O)CH₂(pyrrolidin-1-yl), —NHC(O)CH(NH₂)CH₂CH₂CH₂CH₂N(CH₃)₂, —NHC(O)CH₂N(CH₃)(CH₂CH₃), —NHC(O)CH₂(imidazol-5-yl), —NHC(O)(1-aminocyclopent-1-yl), —NHC(O)CH₂NH(CH₂CH(CH₃)₂), —NHC(O)CH₂N(CH₃)(CH₂CH₃), —NHC(O)(N-(imidazol-4-ylmethyl)-azetidin-3-yl), —NHC(O)(N-ethyl-azetidin-3-yl), —NHCH₂N(CH₃)CH₂CH₂N(CH₃)₂, —NHC(O)CH₂N(CH₃)(N-methyl-pyrrolidin-3-yl), —NHC(O)CH₂N(CH₃)(CH₂CH₂N(CH₃)₂), —NHC(O)CH₂(3-hydroxy-pyrrolidin-1-yl), —NHC(O)(1-amino-cyclobut-1-yl), —NHC(O)CH₂NH(CH₂)₃CH₃, —NHC(O)CH₂(3-piperidin-1-ylazetidin-1-yl), —NHC(O)NH₂, —NHC(O)(1-hydroxycyclopropyl), —NHC(O)CH₂NHN(CH₃)₂, —NHC(O)NH(CH₂)₂N(CH₃)₂, —NHC(O)CH₂ OH, —NHC(O)(pyridazin-4-yl), —NHC(O)(N-methyl-piperidin-4-yl), —NHC(O)CH₂NHCH(CH₃)₃, —NHC(O)CH₂(3-dimethylamino-pyrolidin-1-yl), —NHC(O)CH₂NH(CH₂)₂N(CH₃)₂, —NHC(O)(1-cyclopropylmethyl-azetidin-3-yl), —NHC(O)CH₂NH(CH₃)₃, —NHC(O)(imidazol-2-yl), —NHC(O)(imidazol-4-yl), —NHC(O)(1,2-oxazol-5-yl), —NHC(O)CH₂NHCH₂CF₃, —NHC(O)CH₂CH₂(piperidin-1-yl), —NHC(O)(3-oxo-cyclopent-1-yl), —NHC(O)(2-hydroxy-pyridin-6-yl), —NHC(O)CH₂NH(3-fluoro-4-hydroxyphenyl), —NHC(O)(CH₂)₃N(CH₃)₂, —NHC(O)(1-(furan-2-ylmethyl)-azetidin-3-yl), —NHC(O)(pyrimidin-5-yl), —NHC(O)(pyrrol-2-yl), —NHC(O)CH₂N(CH₃)CH(CH₃)₂, —NHC(O)CH₂N(CH₂CH₃)₂, —NHC(O)CH₂(3-methyl-1,2-oxazol-5-yl), —NHC(O)CH₂NHCH₂(3-hydroxyphenyl), —NHC(O)(N-methyl-pyrrol-2-yl), —NHC(O)(2-amino-tetrahydropyran-2-yl), —NHC(O)CH₂(4-methylamino-piperidin-1-yl), —NHC(O)(piperidin-1-yl), —NHC(O)(N-methyl-pyrrolidin-2-yl), —NHC(O)(thien-3-yl), —NHC(O)(N-(cyclopropylcarbonyl)azetidin-3-yl), —NHC(O)CH₂(4-methylpiperazin-1-yl), —NHC(O)(N-benzylazetidin-3-yl), —NHC(O)(2-chloro-pyridin-3-yl), —NHC(O)CH₂(pyridin-4-yl), —NHC(O)CH₂N(CH₃)(CH₂CH═CH₂), —NHC(O)CH₂NH(benzyl), —NHC(O)CH₂OCH₃, —NHC(O)[1-(C(O)CH₂CH₃)-azetidin-3-yl], —NHC(O)(pyridin-3-yl), —NHC(O)CH₂NHCH₂CH₂OCH₃, —NHC(O)(1-[C(O)CH₃]piperidin-4-yl), —NHC(O)CH₂(2-methyl-pyrrolidin-1-yl), —NHC(O)(furan-3-yl), —NHC(O)CH₂N(CH₃)₂, —NHC(O)(2-chloro-pyridin-5-yl), —NHC(O)(2-chlorophenyl), —NHC(O)CH₂(pyridin-2-yl), —NHC(O)CH₂(3-dimethylamino-azetidin-1-yl), —NHC(O)CH₂(pyridin-3-yl), —NHC(O)CH₂(2-chlorophenyl), —NHC(O)CH₂N(CH₃)CH₂CH₂CH₂N(CH₃)₂, —NHC(O)CH₂N(CH₂CH₃)CH₂CH₂OH, —NHC(O)CH₂(2-benzyl-pyrrolidin-1-yl), —NHC(O)(furan-2-yl, —NHC(O)(2-chloro-pyridin-4-yl), —NHC(O)CH₂NHC(O)CH₃, —NHC(O)CH₂CH₂CH₃, —NHC(O)(4-chlorophenyl), —NHC(O)(4-methyl-phenyl), —NHC(O)CH₂NHC(O)O(CH₃)₃, —NHC(O)(benzo[d][1,3]dioxol-5-yl), —NHC(O)CH₂NHOCH₂(2-methoxyphenyl), —NHC(O)(pyridin-4-yl), —NHC(O)CH_(2[)4-(3,4-dichlorophenyl)-piperazin-1-yl], —NHC(O)CH₂CH₂(pyridin-3-yl), —NHC(O)(tetrahydrofuran-3-yl), —NHC(O)CH₂NHCH₂(2-methylphenyl), —NHC(O)CH(CH₃)CH₂CH₃, —NHC(O)CH₂(3-fluorophenyl), —NHC(O)CH₂C(CH₃)₂-phenyl, —NHC(O)(2-methyl-cycloprop-1-yl), —NHC(O)(2-methyl-4-methoxyphenyl), —NHC(O)(2-methylpyridin-3-yl), —NHC(O)(4-methoxyphenyl), —NHC(O)CH₂(4-ethylpiperazin-1-yl), —NHC(O)(thien-2-yl), —NHC(O)(3-fluoro-2-methylphenyl), —NHC(O)(2-bromo-thien-3-yl), —NHC(O)(4-fluorophenyl), —NHC(O)CH₂(3-methylpiperidin-1-yl), —NHC(O)CH(CH₃)₂, —NHC(O)(CH₂)₃CH₃, —NHC(O)CH₂OCH₂CH₃, —NHC(O)CH₂NH(2-fluorophenyl), —NHC(O)(3-dimethylaminophenyl), —NHC(O)CH₂(4-methylpiperidin-1-yl), —NHC(O)CH₂NH(2-n-propylphenyl), —NHC(O)phenyl, —NHC(O)(pyrazin2-yl), —NHC(O)(3-fluoro-4-methoxyphenyl), —NHC(O)C(CH₃)₂CH₂CH₃, —NHC(O)CH₂O(4-fluorophenyl), —NHC(O)(1-methylcarbonyl-azetidin-3-yl), —NHC(O)CH₂NH(4-methylphenyl), —NHC(O)CH₂NH(phenyl), —NHC(O)CH₂(4-allyl-piperazin-1-yl), —NHC(O)(2-methylphenyl), —NHC(O)CH₂CH₂OCH₃, —NHC(O)(3-methyl-furan-2-yl), —NHC(O)C(CH₃)₃, —NHC(O)CH₂NHObenzyl, —NHC(O)CH₂NH(3-chlorophenyl), —NHC(O)cyclobutyl, —NHC(O)CH₂(3-methoxyphenyl), —NHC(O)(1-methylcycloprop-1-yl), —NHC(O)(3-fluorophenyl), —NHC(O)(4-dimethylaminophenyl), —NHC(O)(3,4-dichlorophenyl), —NHC(O)CH₂NHCH₂(2-methylthiophenyl), —NHC(O)CH₂(2-fluorophenyl), —NHC(O)CH₂N(CH₂CH₃)CH(CH₃)₂, —NHC(O)(thiazol-4-yl), —NHC(O)CH₂N(CH₃)benzyl, —NHC(O)CH₂NHCH₂(thien-2-yl), —NHC(O)CH₂NHCH₂(pyridin-2-yl), —NHC(O)(3-methoxyphenyl), —NHC(O)CH₂NHCH₂(3-chloro-4-methylphenyl), —NHC(O)CH(CH₃)CH₂CH₂CH₃, —NHC(O)CH₂(4-chlorophenyl), —NHC(O)(3-fluoro-4-methylphenyl), —NHC(O)CH₂O(2-methylphenyl), —NHC(O)CH₂(cyclohexyl), —NHC(O)(2-phenyl-cycloprop-1-yl), —NHC(O)(3-chlorophenyl), —NHC(O)CH₂(2-methoxyphenyl), —NHC(O)CH₂CH₂(3-methoxyphenyl), —NHC(O)CH₂NH(2-fluoro-4-methyl-phenyl), —NHC(O)CH₂NHCH₂(3-fluoro-phenyl), —NHC(O)CH₂(4-methoxy-phenyl), —NHC(O)benzyl, —NHC(O)(2,4-dichlorophenyl), —NHC(O)(3-oxo-cyclohex-1-yl), —NHC(O)CH₂NH(3-fluorophenyl), —NHC(O)CH₂(3-chlorophenyl), —NHC(O)CH₂NHCH₂CH(CH₃)phenyl, —NHC(O)CH₂NHCH₂(2,4-dimethylphenyl), —NHC(O)CH₂(2-methyl-piperidin-1-yl), —NHC(O)CH₂NH(2-methoxyphenyl), —NHC(O)CH₂(1,2,3,4-tetrahydroisoquinolin-2-yl), —NHC(O)CH₂CH₂CH═CH₂, —NHC(O)CH₂NH(2-methylphenyl), —NHC(O)CH₂(4-oxo-piperidin-1-yl), —NHC(O)(2-fluorophenyl), —NHC(O)CH₂NHCH(CH₃)phenyl, —NHC(O)(2-fluoro-6-methoxyphenyl), —NHC(O)CH₂NH(2-isopropylphenyl), —NHC(O)CH₂CH₂(2-methoxyphenyl), —NHC(O)CH₂CH₂CH(CH₃)₂, —NHC(O)CH₂(2-phenyl-morpholin-4-yl), —NHC(O)CH₂CH₂(4-methoxyphenyl), —NHC(O)CH₂N(allyl)cyclopentyl, —NHC(O)CH₂N(CH₃)CH₂CH₂OCH₃, —NHC(O)CH₂CH₂C(O)cyclopropyl, —NHC(O)CH₂NH(3-tert-butylphenyl), —NHC(O)CH₂N(n-propyl)(cyclopropylmethyl), —NHC(O)CH₂(2-oxo-cyclopentyl), —NHC(O)CH₂NH(4-chlorophenyl), —NHC(O)CH₂(4-piperidin-1-ylpiperidin-1-yl), —NHC(O)CH₂(4-cyclopentylpiperazin-1-yl), —NHC(O)CH₂(2-methylphenyl), —NHC(O)CH₂NHCH₂(3-fluoro-6-methylphenyl), —NHC(O)CH₂C(CH₃)₃, —NHC(O)CH₂NH(2-chlorophenyl), —NHC(O)(3-fluoro-6-methylphenyl), —NHC(O)(4-fluoro-3-methylphenyl), —NHC(O)(2,3-dichlorophenyl), —NHC(O)CH₂O phenyl, —NHC(O)CH₂NH(2,3-dimethylphenyl), —NHC(O)(2-fluoro-5-methylphenyl), —NHC(O)CH₂NHOCH₂(4-methylphenyl), —NHC(O)CH₂(4-isopropylpiperazin-1-yl), —NHC(O)CH₂(4-fluorophenyl), —NHC(O)CH₂CH(CH₃)₂, —NHC(O)(2-methoxy-4-methylphenyl), —NHC(O)CH₂(4-n-propylpiperidin-1-yl), —NHC(O)CH₂O(3-methylphenyl), —NHC(O)(tetrahydrofuran-2-yl), —NHC(O)CH₂(3-hydroxymethylpiperidin-1-yl), —NHC(O)(1-tert-butoxycarbonylpiperidin-2-yl), —NHC(O)CH₂N(CH₃)CH₂(pyridin-3-yl), —NHC(O)CH₂N(CH₂CH₃)phenyl, —NHC(O)CH₂OCH₂CH₂OCH₃, —NHC(O)CH₂CH₂(cyclopentyl), —NHC(O)(2,5-dichlorophenyl), —NHC(O)CH₂(4-methylcarbonylpiperazin-1-yl), —NHC(O)(5-fluoro-2-methoxyphenyl), —NHC(O)CH₂N(CH₂CH₃)cyclohexyl, —NHC(O)(5-methyl-1,2-oxazol-3-yl), —NHC(O)(3-methylpyridin-3-yl), —NHC(O)(2-methoxypyridin-3-yl), —NHC(O)(3,5-dichlorophenyl), —NHC(O)CH₂(thiazolidin3-yl), —NHC(O)CH₂(4-[C(O)H]-piperazin-1-yl), —NHC(O)CH₂(2-pyridin-4-ylpiperidin-1-yl), —NHC(O)(2-methoxyphenyl), —NHC(O)CH₂N(CH₃)CH₂CH(CH₃)₂, —NHC(O)CH₂(4-[C(O)H]-homopiperazin-1-yl), —NHC(O)(1-phenylcycloprop-1-yl), —NHC(O)CH₂(2,6-dimethylmorpholin-4-yl), NHC(O)CH₂(2-phenylpyrrolidin-1-yl), —NHC(O)CH₂(morpholin-4-yl), —C(O)NHCH(CH₃)CH₂N(CH₃)₂, —C(O)NHCH₂CH₂N(CH₃)₂, —C(O)NH(pyrrolidin-3-yl), —C(O)NHCH₂CH₂(pyrrolidin-1-yl), —C(O)NHCH₂CH₂NH₂, —C(O)N(CH₃)CH₂CH₂N(CH₃)₂, —C(O)NHCH₂(piperidin-2-yl), —C(O)NH(1-methylazetidin-3-yl), —C(O)NHCH₂CH₂(piperidin-1-yl), —C(O)NHCH₂CH₂N(CH₂CH₃)₂, —C(O)NH(1-methylpiperidin-3-yl), —C(O)NH(piperidin-3-yl), —C(O)NHCH₂(1-methylpiperidin-3-yl), —C(O)NHCH₂CH₂N(CH₂CH₂OH)₂, —C(O)NH(1-ethylpiperidin-3-yl), —C(O)NH₂, —C(O)(3-aminopyrrolidin-1-yl), —C(O)(3-methylaminopyrrolidin-1-yl), —C(O)OH, —C(O)NHCH₂CH₂(morpholin-4-yl), —C(O)NHCH₂(1-ethylpyrrolidin-2-yl), —C(O)(4-amino-3-oxo-pyrazolidin-1-yl), —C(O)NHCH₃, —C(O)(3-aminocyclobut-1-yl), —C(O)NHCH₂(pyridin-3-yl), —C(O)NHCH₂CH₂OH, —C(O)NH(3-oxo-pyrazolidin-4-yl), —NHCH₂CH₂(imidazol-4-yl), —C(O)(3-dimethylaminopyrrolidin-1-yl), —C(O)NHCH₂(pyridin-4-yl), —C(O)N(CH₃)(1-methyl-pyrrolidin-3-yl), —C(O)(3-diethylaminopyrrolidin-1-yl), —C(O)NH(pyrrol-1-yl), —C(O)NHCH₂CH₂CH₂(pyrrolidin-1-yl), —C(O)N(CH₃)CH₂CH₂CN, —C(O)NHCH₂CH₂OCH₃, —C(O)N(CH₂CH₃)CH₂CH₂CN, —C(O)(3-aminopiperidin-1-yl), —C(O)NHCH₂CH₂CH₂N(CH₃)₂, —C(O)NH(morpholin-4-yl), —C(O)NHN(CH₃)₂, —C(O)NHCH₂CH₂CH₂(imidazol-1-yl), —C(O)NHCH₂CH₂CH₂N(CH₂CH₃)₂, —C(O)NHCH₂CH₂CN, —C(O)NHCH₂CH₂C(O)OCH₃, —C(O)NHCH₂CH₂SCH₃, —C(O)NHCH₂CH₂SCH₂CH₃, —C(O)N(CH₂CH₃)CH₂CH₂N(CH₃)₂, —C(O)NHCH₂CH₂CH₂(2-oxo-pyrrolidin-1-yl), —C(O)NHCH₂CH₂(pyridin-4-yl), —C(O)NHCH₂CH₂CH₂OCH₂CH₃, —C(O)NHCH₂CH₂CH₂(morpholin-4-yl), —C(O)NHCH₂CH₂CH₂OCH₃, —C(O)N(CH₃)CH₂CH₂CH₂N(CH₃)₂, —C(O)NHCH₂CH₂CH₂OCH₂CH₂CH₃, —C(O)NHCH₂CH₂C(O)OCH₂CH₃, —C(O)NHCH₂CH₂CH₂OCH(CH₃)₂, —C(O)NHC(CH₃)₂CH₂(piperidin-1-yl), —C(O)N(CH₃)CH₂CH₂CH₃, —C(O)NH(piperidin-1-yl), —C(O)NHCH(CH₃)CH₂OCH₃, —C(O)NHC(CH₃)₂CH₂(morpholin-4-yl), —C(O)(2-dimethylaminomethylpiperidin-1-yl), —C(O)NH(CH₂)₃—O—(CH₂)₃CH₃, —C(O)NHCH(CH₃)(CH₂)₃N(CH₂CH₃)₂, —C(O)NHC(CH₃)₂C(O)(piperidin-1-yl), —C(O)(4-methylpiperazin-1-yl), —C(O)(2-piperidin-1-ylmethyl-piperidin-1-yl), cyano, —NHCH₃, —CH(CH₃)NHCH₂CH₂N(CH₃)₂, —C(O)CH₃, —S(O)₂NHCH₂CH₂N(CH₃)₂, —S(O)₂NH(CH₂)₃N(CH₃)₂, 5-(N,N-dimethylaminomethyl)-1,3,4-oxadiazol-2-yl, —NHCH₂CH₂N(CH₃)₂, —N(CH₃)₂, —OCH₂CH₂N(CH₃)₂, —NHC[N(CH₃)₂][═N(CH₃)₂], —OCH F₂, —CF₃, —S(O)₂CH₃, —OCF₃, —NHC(O)CH₂(4-dimethylaminopiperidin-1-yl), or methoxy.

In another embodiment (P), the Compound of Formula I is that where each R³ is independently halo, alkyl, hydroxyamino, —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)), —C(O)NR⁸R^(8a), —NR⁹C(O)R^(9a), —C(O)N(R¹⁰)—C₁-C₆-alkylene-N(R^(10a))R^(10b)—NR¹¹C(O)NR^(11a)R^(11b), —N(R²²)C(O)—C₁-C₆-alkylene-N(R^(22b))— NR^(22c))(R^(22a)), —NR¹³C(O)OR^(13a), —N(R¹⁸)C(O)—C₁-C₆-alkylene-N(R^(18b))C(O)R^(18a), —NR²⁴C(O)—C₁₋C₆-alkylene-OR^(24a), or —N(R²⁰)C(O)—C₁-C₆-alkylene-C(O)R^(20a); where each of the alkylene in R³ is independently optionally further substituted with 1, 2, 3, 4, or 5 groups selected from halo, hydroxy, and amino; and all other groups are as defined in the Summary of the Invention. In another embodiment, each R³ is independently methyl, chloro, —NHC(O)CH₂NH(CH₃), —NHC(O)CH(CH₃)NH₂, —NHC(O)C(CH₃)₂NH₂, —NHC(O)CH₂N(CH₃)₂, —NHC(O)CH₂N(CH₃)CH₂CH₂N(CH₃)₂, —NHC(O)CH(NH₂)CH₂CH₃, —NHC(O)CH₂N(CH₃)CH₂CH₂N(CH₃)₂, —NHC(O)CH(CH₃)NH(CH₃), —NHC(O)H, —NHC(O)CH₂(azetidin-1-yl), —NHC(O)(pyrrolidin-2-yl), —NHC(O)CH(NH₂)CH₂OH, —NHC(O)(azetidin-4-yl), —NHC(O)C(CH₃)₂NH(CH₃), —NH₂, —NHC(O)CH₂NH(CH₂CH₂CH₃), —NHC(O)CH₂CH₂NH₂, —NHOH, or —NHC(O)(piperidin-3-yl).

In another embodiment (Q), the Compound of Formula I is that where R³ is alkyl or —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)); and R⁷ is hydrogen or alkyl and R^(7a) and R^(7b) are independently hydrogen, alkyl, aminoalkyl, alkylaminoalkyl, or dialkylaminoalkyl; and all other groups are as defined in the Summary of the Invention. In another embodiment, each R³ is independently methyl, —NHC(O)CH₂NH(CH₃), —NHC(O)CH(CH₃)NH₂, —NHC(O)C(CH₃)₂NH₂, —NHC(O)—CH₂N(CH₃)₂, —NHC(O)CH₂N(CH₃)CH₂CH₂N(CH₃)₂, —NHC(O)CH(NH₂)CH₂CH₃, —NHC(O)CH₂N(CH₃)CH₂CH₂N(CH₃)₂, or —NHC(O)CH(CH₃)NH(CH₃).

In another embodiment (R), the Compound of Formula I is that where B is phenyl, R³ is not present or R³ is halo, alkyl, or alkoxy; R^(3a) is —C(O)NR⁸R^(8a), —NR⁹C(O)R^(9a), —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)), or —C(O)N(R¹⁰)—C₁-C₆-alkylene-N(R^(10a))R^(10b) where each of the alkylene in R^(3a) is independently optionally further substituted with 1, 2, 3, 4, or 5 groups selected from halo, hydroxy, and amino; and all other groups are as defined in the Summary of the Invention.

In another embodiment (R1) of embodiment R, the compound is that where R⁵⁰, R⁵², and R⁵³ are hydrogen and R⁵⁴ is halo or alkoxy; R⁵⁰, R⁵², and R⁵⁴ are hydrogen and R⁵³ is alkoxy; or R⁵⁰ and R⁵² are hydrogen and R⁵³ and R⁵⁴ together with the carbons to which they are attached form a 6-membered heteroaryl; and all other groups are as defined in the Summary of the Invention. In another embodiment, R⁵⁰, R⁵², and R⁵³ are hydrogen and R⁵⁴ is halo or alkoxy; or R⁵⁰, R⁵², and R⁵⁴ are hydrogen and R⁵³ is alkoxy.

In another embodiment of (R²) of embodiment R, the compound is that where R⁵¹ is methyl.

In another embodiment (S), the compound of Formula Ia:

is that where R³ is not present or R³ is alkyl and R^(3a) is —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)), —C(O)NR⁸R^(8a), —NR⁹C(O)R^(9a), or)-C(O)N(R¹⁰)—C₁-C₆-alkylene-N(R^(10a))R^(10b); where each of the alkylene in R^(3a) is independently optionally further substituted with 1, 2, 3, 4, or 5 groups selected from halo, hydroxy, and amino; and all other groups are as defined in the Summary of the Invention. In another embodiment, R³ is not present or is methyl. In another embodiment, R³ is not present.

In another embodiment (S1) of embodiment S is that where R⁷ is hydrogen or alkyl and R^(7a), and R^(7b) are independently hydrogen, alkyl, hydroxyalkyl, aminoalkyl, alkylaminoalkyl, or dialkylaminoalkyl; R⁸ is hydrogen or alkyl and R^(8a) is heterocycloalkyl or heterocycloalkylalkyl; R⁹ is hydrogen or alkyl and R^(9a) is hydrogen, heterocycloalkyl, or heterocycloalkylalkyl; and R¹⁰, R^(10a), and R^(10b) are independently hydrogen, alkyl, hydroxyalkyl, aminoalkyl, alkylaminoalkyl, or dialkylaminoalkyl.

In another embodiment (S2) of embodiment S is that where R⁵⁰, R⁵², and R⁵³ are hydrogen and R⁵⁴ is halo or alkoxy; or R⁵⁰, R⁵², and R⁵⁴ are hydrogen and R⁵³ is alkoxy; or R⁵⁰ and R⁵² are hydrogen and R⁵³ and R⁵⁴ together with the carbons to which they are attached form a 6-membered heteroaryl. In another embodiment, R⁵⁰, R⁵², and R⁵³ are hydrogen and R⁵⁴ is halo or alkoxy; or R⁵⁰, R⁵², and R⁵⁴ are hydrogen and R⁵³ is alkoxy.

In another embodiment of (S3) of embodiment S, the compound is that where R⁵¹ is methyl.

In another embodiment (T), the Compound of Formula I is that where B is heteroaryl, one R³ is halo, alkyl, or alkoxy and a second R³ is —C(O)NR⁸R^(8a), —NR⁹C(O)R^(9a), —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)), or)-C(O)N(R¹⁰)—C₁-C₆-alkylene-N(R^(10a))R^(10b) where each of the alkylene in R³ is independently optionally further substituted with 1, 2, 3, 4, or 5 groups selected from halo, hydroxy, and amino; and all other groups are as defined in the Summary of the Invention.

In another embodiment (T1) of embodiment T, the compound is that where R⁷ is hydrogen or alkyl and R^(7a), and R^(1b) are independently hydrogen, alkyl, hydroxyalkyl, aminoalkyl, alkylaminoalkyl, or dialkylaminoalkyl; R⁸ is hydrogen or alkyl and R^(8a) is heterocycloalkyl or heterocycloalkylalkyl; R⁹ is hydrogen or alkyl and R^(9a) is hydrogen, heterocycloalkyl, or heterocycloalkylalkyl; R¹⁰, R^(10a), and R^(10b) are independently hydrogen, alkyl, hydroxyalkyl, aminoalkyl, alkylaminoalkyl, or dialkylaminoalkyl.

In another embodiment U, the compound of Formula I is that where B is

each R³ (when R³ is present) is independently halo, alkyl, alkoxy, aminoalkyloxy, alkylaminoalkyloxy, dialkylaminoalkyloxy, alkylamino, dialkylamino, —C(O)NR⁸R^(8a), —NR⁹C(O)R^(9a), —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)), or —C(O)N(R¹⁰)—C₁-C₆-alkylene-N(R^(10a))R^(10b); and all other groups are as defined in the Summary of the Invention.

In another embodiment (U1) of embodiment U, the compound of Formula I is that where R⁵⁰, R⁵², and R⁵³ are hydrogen and R⁵⁴ is halo or alkoxy; R⁵⁰, R⁵², and R⁵⁴ are hydrogen and R⁵³ is alkoxy; or R⁵⁰ and R⁵² are hydrogen and R⁵³ and R⁵⁴ together with the carbons to which they are attached form a 6-membered heteroaryl; and all other groups are as defined in the Summary of the Invention. In another embodiment, R⁵⁰, R⁵², and R⁵³ are hydrogen and R⁵⁴ is halo or alkoxy; or R⁵⁰, R⁵², and R⁵⁴ are hydrogen and R⁵³ is alkoxy.

In another embodiment (U2) of embodiment U1, the compound of Formula I is that where R⁵¹ is methyl.

In another embodiment (U3) of embodiment U, the Compound of Formula I is that where R⁷ is hydrogen or alkyl and R^(7a), and R^(7b) are independently hydrogen, alkyl, hydroxyalkyl, aminoalkyl, alkylaminoalkyl, or dialkylaminoalkyl; R⁸ is hydrogen or alkyl and R^(8a) is heterocycloalkyl or heterocycloalkylalkyl; R⁹ is hydrogen or alkyl and R^(9a) is hydrogen, heterocycloalkyl, or heterocycloalkylalkyl; R¹⁰, R^(10a), and R^(10b) are independently hydrogen, alkyl, hydroxyalkyl, aminoalkyl, alkylaminoalkyl, or dialkylaminoalkyl

In another embodiment of the Invention (V) the Compound of Formula I is that where W¹, W², W³, and W⁴ are —C(H)═; or W² and W³ are —C(H)═ and one of W¹ and W⁴ is —N═ and the other is —C(H)═;

-   R⁵⁰ is hydrogen; -   R⁵¹ is hydrogen or alkyl; -   R⁵² is hydrogen; -   R⁵³ is hydrogen, alkoxy, nitro, amino, or     —N(R⁵⁵)C(O)—C₁-C₆-alkylene-N(R^(55a))R^(55b); and R⁵⁴ is hydrogen,     alkyl, alkoxy, or halo; or R⁵³ and R⁵⁴ together with the carbons to     which they are attached form a 6-membered heteroaryl; -   B is phenyl substituted with R^(3a) and optionally further     substituted with one R³; or -   B is heteroaryl optionally substituted with one or two R³; -   R^(3a) is cyano; hydroxyamino; carboxy; alkylsulfonyl,     aminoalkyloxy; alkylaminoalkyloxy; dialkylaminoalkyloxy;     —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)); —C(O)NR⁸R^(8a);     —NR⁹C(O)R^(9a); —C(O)N(R¹⁰)—C₁-C₆-alkylene-N(R^(10a))R^(10b);     —NR¹¹C(O)NR^(11a)R^(11b) where R^(11a); —C(O)R¹²; —NR¹³C(O)OR^(13a);     —C(O)N(R¹⁴)N(R^(14a))(R^(14b));     —S(O)₂N(R¹⁵)—C₁-C₆-alkylene-N(R^(15a))R^(15b);     —C(O)N(R¹⁶)—C₁-C₆-alkylene-C(O)OR^(16a); heteroaryl optionally     substituted with one or two aminoalkyl, alkylaminoalkyl, or     dialkylaminoalkyl; —N(R¹⁷)—     C(═N(R^(17b))(R^(17a)))(NR^(17c)R^(17d));     —N(R¹⁸)C(O)—C₁-C₆-alkylene-N(R^(18b))C(O)R^(18a);     —C(O)N(R¹⁹)—C₁-C₆-alkylene-C(O)R^(19a);     —N(R²²)C(O)—C₁-C₆-alkylene-N(R^(22b))—N(R^(22c))(R^(22a));     —C₀₋C₆-alkylene-N(R²³)—C₁₋C₆-alkylene-N(R^(23b))R^(23a); or     —NR²⁴C(O)—C₁₋C₆-alkylene-OR^(24a); where each of the alkylene in     R^(3a) is independently optionally further substituted with 1, 2, 3,     4, or 5 groups selected from halo, hydroxy, and amino; -   each R³ (when R³ is present) is independently halo; cyano; alkyl;     alkenyl; alkoxy; hydroxyamino; carboxy; alkylsulfonyl,     aminoalkyloxy; alkylaminoalkyloxy; dialkylaminoalkyloxy;     —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)); —C(O)NR⁸R^(8a);     —NR⁹C(O)R^(9a); —C(O)N(R¹⁰)—C₁-C₆-alkylene-N(R^(10a))R^(10b);     —NR¹¹C(O)NR^(11a)R^(11b) where R^(11a); —C(O)R¹²; —NR¹³C(O)OR^(13a);     —C(O)N(R¹⁴)N(R^(14a))(R^(14b));     S(O)₂N(R¹⁵)—C₁-C₆-alkylene-N(R^(15a))R^(15b);     —C(O)N(R¹⁶)—C₁-C₆-alkylene-C(O)OR^(16a); heteroaryl optionally     substituted with one or two aminoalkyl, alkylaminoalkyl, or     dialkylaminoalkyl; —N(R¹⁷)— C(═N(R¹⁷NR^(17a)))(NR^(17c)R^(17d));     —N(R¹⁸)C(O)—C₁-C₆-alkylene-N(R^(18b))C(O)R^(18a);     —C(O)N(R¹⁹)—C₁-C₆-alkylene-C(O)R^(19a);     —N(R²²)C(O)—C₁-C₆-alkylene-N(R^(22b))—N(R^(22c))(R^(22a));     —N(R^(23b))R^(23a); or     —NR²⁴C(O)—C₁₋C₆-alkylene-N(R²³)—C₁₋C₆-alkylene or     —NR²⁴C(O)—C₁₋C₆-alkylene-OR^(24a); where each of the alkylene in R³     is independently optionally further substituted with 1, 2, 3, 4, or     5 groups selected from halo, hydroxy, and amino; -   provided that when R⁵⁰ and R⁵² are hydrogen, R⁵¹ is hydrogen or     methyl, R⁵³ is hydrogen or methoxy, and R⁵⁴ is hydrogen or methoxy,     then B is not 2,3-dihydro-1,4-benzodioxinyl, thien-2-yl, or     thien-2-yl substituted with one R³ where R³ is halo.

Another embodiment (W) of the invention is a Compound of Formula I where R⁵⁰, R⁵³, and R⁵⁴ are independently hydrogen, alkyl, alkenyl, halo, haloalkyl, haloalkenyl, hydroxy, alkoxy, alkenyloxy, haloalkoxy, nitro, amino, alkylamino, dialkylamino, —N(R⁵⁵)C(O)—C₁-C₆-alkylene-N(R^(55a))R^(55b), alkylcarbonyl, alkenylcarbonyl, carboxy, alkoxycarbonyl, cyano, alkylthio, —S(O)₂NR⁵⁵R^(55a), or alkylcarbonylamino and where R⁵⁵ and R^(55b) are independently hydrogen, alkyl, or alkenyl and R^(55a) is hydrogen, alkyl, alkenyl, hydroxy, or alkoxy; or R⁵³ and R⁵⁴ together with the carbons to which they are attached form a 5- or 6-membered heteroaryl or 5- or 6-membered heterocycloalkyl.

Another embodiment (X) of the invention is a Compound of Formula I where R⁵³ and R⁵⁴ together with the carbons to which they are attached form a 5- or 6-membered heteroaryl or 5- or 6-membered heterocycloalkyl.

Representative Compounds

Representative compounds of Formula I and/or II are depicted below. The examples are merely illustrative and do not limit the scope of the invention in any way. Compounds of the invention are named according to systematic application of the nomenclature rules agreed upon by the International Union of Pure and Applied Chemistry (IUPAC), International Union of Biochemistry and Molecular Biology (IUBMB), and the Chemical Abstracts Service (CAS). Names in Table 1 were generated using ACD/Labs naming software 8.00 release, product version 8.08 with the exception of Compound 374 which was named using ChemDraw v. 9.0.1.

Table 1 Representative PI3K-Alpha Inhibitors

The Compounds in Table 1 can be prepared as pharmaceutically acceptable salts, solvates, hydrates, and/or isomers thereof. All such salt, solvate, hydrate, and isomer combinations of the Compounds in Table 1 can be used to practice the invention. In particular, the invention can be practiced with one or two pharmaceutically acceptable salts of a Compound of Table 1 which salt(s) are formed with one or two acids independently selected from hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, acetic acid, trifluoroacetic acid, propionic acid, hexanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, 3-(4-hydroxybenzoyl)benzoic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, 1,2-ethanedisulfonic acid, 2-hydroxyethanesulfonic acid, benzenesulfonic acid, 4-chlorobenzenesulfonic acid, 2-naphthalenesulfonic acid, 4-toluenesulfonic acid, camphorsulfonic acid, glucoheptonic acid, 4,4′-methylenebis-(3-hydroxy-2-ene-1-carboxylic acid), 3-phenylpropionic acid, trimethylacetic acid, tertiary butylacetic acid, lauryl sulfuric acid, gluconic acid, glutamic acid, hydroxynaphthoic acid, salicylic acid, stearic acid, muconic acid, p-toluenesulfonic acid, and salicylic acid. In particular, the invention can be practiced with one or two pharmaceutically acceptable salts of a Compound of Table 1 which salt(s) are formed with one or two bases independently selected from sodium, potassium, lithium, ammonium, calcium, magnesium, iron, zinc, copper, manganese, aluminum, isopropylamine, trimethylamine, diethylamine, triethylamine, tripropylamine, ethanolamine, 2-dimethylaminoethanol, 2-diethylaminoethanol, dicyclohexylamine, lysine, arginine, histidine, caffeine, procaine, hydrabamine, choline, betaine, ethylenediamine, glucosamine, methylglucamine, theobromine, purines, piperazine, piperidine, N-ethylpiperidine, tromethamine, and N-methylglucamine. Any individual compound (and any optional salt, optional solvate, and optional hydrate thereof) in Table 1 can be used in combination with any of the above embodiments.

TABLE 1 Cpd. No. Structure Name 1

N-(4-{[(3-{[4-(methoxy)phenyl] amino}quinoxalin-2-yl) amino]sulfonyl}phenyl) acetamide 2

4-bromo-N-[3-(phenylamino) quinoxalin-2-yl]benzene sulfonamide 3

4-bromo-N-{3-[(2- methylphenyl)amino] quinoxalin-2-yl}benzene sulfonamide 4

4-bromo-N-(3-{[4- (methoxy)phenyl]amino} quinoxalin-2-yl)benzene sulfonamide 5

4-chloro-N-{3-[(4- chlorophenyl)amino]-6- (methoxy)quinoxalin-2- yl}benzenesulfonamide 6

N-(4-{[3-{[(4-chlorophenyl) sulfonyl]amino}-7-(methoxy) quinoxalin-2-yl]amino} phenyl)acetamide 7

4-chloro-N-{6-(methoxy)-3-[(2- oxo-2,3-dihydro-1H- benzimidazol-5-yl)amino] quinoxalin-2-yl} benzenesulfonamide 8

N-{4-[(3-{[(4-chlorophenyl) sulfonyl]amino}quinoxalin-2- yl)amino]phenyl}acetamide 9

N-(3-{[4-(ethyloxy)phenyl] amino}quinoxalin-2-yl)-4- methylbenzene sulfonamide 10

N-{3-[(3,4-dimethylphenyl) amino]-6-methylquinoxalin- 2-yl}-4-methylbenzene sulfonamide 11

N-(3-{[3-(dimethylamino) phenyl]amino}quinoxalin-2- yl)-4-methylbenzene sulfonamide 12

4-methyl-N-{6-methyl-3-[(4- methylphenyl)amino]quinoxalin- 2-yl} benzene sulfonamide 13

N-{3-[(4-hydroxyphenyl) amino]-6-methylquinoxalin- 2-yl}-4-methylbenzene sulfonamide 14

N-{3-[(2,5-dimethylphenyl) amino]quinoxalin-2-yl}-4- methylbenzenesulfonamide 15

4-chloro-N-[3-(naphthalen- 2-ylamino)quinoxalin-2- yl]benzenesulfonamide 16

N-{3-[(3-aminophenyl)amino] quinoxalin-2-yl}-4- chlorobenzenesulfonamide 17

N-(3-{[4-(aminosulfonyl)phenyl] amino}quinoxalin-2-yl)-3- nitrobenzenesulfonamide 18

4-chloro-N-{3-[(4-chlorophenyl) amino]quinoxalin-2-yl} benzenesulfonamide 19

4-chloro-N-{3-[(4-methylphenyl) amino]quinoxalin-2-yl} benzenesulfonamide 20

4-chloro-N-{3-[(2-methylphenyl) amino]quinoxalin-2-yl} benzenesulfonamide 21

methyl 4-[(3-{[(4-chlorophenyl) sulfonyl]amino} quinoxalin-2- yl)amino]benzoate 22

methyl 2-chloro-5-[(3-{[(4- methylphenyl)sulfonyl]amino} quinoxalin-2-yl)amino]benzoate 23

N-{4-[(7-methyl-3-{[(4- methylphenyl)sulfonyl]amino} quinoxalin-2-yl) amino]phenyl}acetamide 24

4-methyl-N-(6-methyl-3-{[2- (methoxy)phenyl]amino} quinoxalin-2-yl) benzenesulfonamide 25

N-{3-[(phenylmethyl) amino]quinoxalin-2-yl} benzenesulfonamide 26

4-({3-[(phenylsulfonyl)amino] quinoxalin-2-yl}amino) benzoic acid 27

3-({3-[(phenylsulfonyl)amino] quinoxalin-2-yl}amino) benzenesulfonamide 28

N-{3-[(1,5-dimethyl-3-oxo-2- phenyl-2,3-dihydro-1H-pyrazol- 4-yl)amino]quinoxalin-2-yl} benzenesulfonamide 29

N-{3-[(4-hydroxyphenyl) amino]quinoxalin-2-yl} benzenesulfonamide 30

N-{3-[(4-hydroxyphenyl) amino]quinoxalin-2-yl}-4- methylbenzenesulfonamide 31

N-(3-{[4-(aminosulfonyl)phenyl] amino}quinoxalin-2-yl)-4- methylbenzenesulfonamide 32

3-[(3-{[(4-methylphenyl) sulfonyl]amino}quinoxalin-2- yl)amino]benzoic acid 33

N-[4-({[3-(phenylamino) quinoxalin-2-yl]amino}sulfonyl) phenyl]acetamide 34

N-(4-{[(3-{[4-(aminosulfonyl) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl) acetamide 35

N-[4-({[3-(naphthalen-1- ylamino)quinoxalin-2-yl] amino}sulfonyl)phenyl] acetamide 36

N-{4-[(3-{[(4-methylphenyl) sulfonyl]amino}quinoxalin-2- yl)amino]phenyl}acetamide 37

N-(3-{[3-(aminosulfonyl) phenyl]amino}quinoxalin-2-yl)- 4-bromobenzenesulfonamide 38

N-{3-[(3-hydroxyphenyl)amino] quinoxalin-2-yl}-4- methylbenzenesulfonamide 39

4-[(3-{[(4-chlorophenyl) sulfonyl]amino}quinoxalin-2- yl)amino]-2-hydroxybenzoic acid 40

N-(3-{[4-(methoxy)phenyl] amino}quinoxalin-2-yl)-3- nitrobenzenesulfonamide 41

3-[(3-{[(4-chlorophenyl) sulfonyl]amino}quinoxalin- 2-yl)amino]benzoic acid 42

N-(3-{[4-(aminosulfonyl) phenyl]amino}quinoxalin-2-yl)- 4-chlorobenzenesulfonamide 43

N-(3-{[3-(aminosulfonyl) phenyl]amino}quinoxalin-2-yl)- 4-chlorobenzenesulfonamide 44

N-[3-(naphthalen-2-ylamino) quinoxalin-2-yl]-4- nitrobenzenesulfonamide 45

N-(3-{[3-(methoxy)phenyl] amino}quinoxalin-2-yl) benzenesulfonamide 46

N-{3-[(4-bromophenyl)amino] quinoxalin-2-yl}-3- nitrobenzenesulfonamide 47

3-[(3-{[(4-nitrophenyl)sulfonyl] amino}quinoxalin-2- yl)amino]benzoic acid 48

4-nitro-N-[3-(phenylamino) quinoxalin-2-yl] benzenesulfonamide 49

4-chloro-N-[3- (phenylamino)quinoxalin- 2-yl]benzenesulfonamide 50

3-nitro-N-[3-(phenylamino) quinoxalin-2-yl] benzenesulfonamide 51

4-[(3-{[(4-nitrophenyl)sulfonyl] amino}quinoxalin-2-yl)amino] benzoic acid 52

N-[3-(naphthalen-2-ylamino) quinoxalin-2-yl]-3- nitrobenzenesulfonamide 53

4-methyl-N-(3-{[3-(methoxy) phenyl]amino}quinoxalin-2-yl) benzenesulfonamide 54

N-(3-{[3-chloro-4-(methoxy) phenyl]amino}quinoxalin-2- yl)benzenesulfonamide 55

N-{3-[(3-chloro-4-fluorophenyl) amino]quinoxalin-2-yl} benzenesulfonamide 56

methyl 2-chloro-5-({3- [(phenylsulfonyl)amino] quinoxalin-2-yl}amino)benzoate 57

4-chloro-N-{3-[(3- hydroxyphenyl)amino]quinoxalin- 2-yl}benzenesulfonamide 58

4-methyl-N-[6-methyl-3- (phenylamino)quinoxalin-2-yl] benzenesulfonamide 59

N-{4-[({3-[(4-methylphenyl) amino]quinoxalin-2-yl}amino) sulfonyl]phenyl}acetamide 60

1-methylethyl 4-[(3-{[(4- chlorophenyl)sulfonyl] amino}-7-methylquinoxalin- 2-yl)amino]benzoate 61

N-{3-[(4-methylphenyl)amino] quinoxalin-2-yl} benzenesulfonamide 62

N-{3-[(3-methylphenyl)amino] quinoxalin-2-yl} benzenesulfonamide 63

N-{3-[(4-bromophenyl)amino] quinoxalin-2-yl}-4- methylbenzenesulfonamide 64

4-methyl-N-{3-[(3-methylphenyl) amino]quinoxalin-2-yl} benzenesulfonamide 65

4-methyl-N-[3-(naphthalen-1- ylamino)quinoxalin-2-yl] benzenesulfonamide 66

N-{4-[({3-[(4-chlorophenyl) amino]quinoxalin-2-yl}amino) sulfonyl]phenyl}acetamide 67

N-(4-{[(3-{[3-(aminosulfonyl) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl) acetamide 68

4-methyl-N-{3-[(phenylmethyl) amino]quinoxalin-2-yl} benzenesulfonamide 69

4-[(3-{[(4-bromophenyl) sulfonyl]amino}quinoxalin- 2-yl)amino]-2- hydroxybenzoic acid 70

4-bromo-N-{3-[(4- methylphenyl)amino]quinoxalin- 2-yl}benzenesulfonamide 71

4-bromo-N-{3-[(3-methylphenyl) amino]quinoxalin-2-yl} benzenesulfonamide 72

N-{4-[({3-[(2-hydroxyethyl) amino]quinoxalin-2-yl}amino) sulfonyl]phenyl}acetamide 73

4-bromo-N-[3-(naphthalen- 1-ylamino)quinoxalin-2-yl] benzenesulfonamide 74

4-[(3-{[(4-chlorophenyl) sulfonyl]amino}quinoxalin-2- yl)amino]benzoic acid 75

3-[(3-{[(3-nitrophenyl)sulfonyl] amino}quinoxalin-2-yl)amino] benzoic acid 76

N-{3-[(2-methylphenyl)amino] quinoxalin-2-yl} benzenesulfonamide 77

4-({3-[(phenylsulfonyl)amino] quinoxalin-2-yl}amino) benzenesulfonamide 78

N-[3-(naphthalen-1-ylamino) quinoxalin-2-yl]-3- nitrobenzenesulfonamide 79

N-(3-{[3-(aminosulfonyl) phenyl]amino}quinoxalin-2-yl)- 3-nitrobenzenesulfonamide 80

N-{3-[(4-bromophenyl)amino] quinoxalin-2-yl}-4- nitrobenzenesulfonamide 81

4-chloro-N-[3-(naphthalen-1- ylamino)quinoxalin-2-yl] benzenesulfonamide 82

N-{4-[({3-[(phenylmethyl) amino]quinoxalin-2-yl}amino) sulfonyl]phenyl}acetamide 83

N-[4-({[3-(butylamino) quinoxalin-2-yl]amino} sulfonyl)phenyl]acetamide 84

N-[3-(butylamino)quinoxalin-2- yl]-4-methylbenzenesulfonamide 85

N-[3-(cyclohexylamino) quinoxalin-2-yl] benzenesulfonamide 86

1-(phenylsulfonyl)-3-[4- (pyrrolidin-1-ylsulfonyl) phenyl]-2,3-dihydro-1H- imidazo[4,5-b]quinoxaline 87

1-(phenylsulfonyl)-3-[4- (piperidin-1-ylsulfonyl)phenyl]- 2,3-dihydro-1H-imidazo[4,5-b] quinoxaline 88

2,5-dichloro-N-[3-(3,4- dihydroquinolin-1(2H)- yl)quinoxalin-2-yl] benzenesulfonamide 89

ethyl 2-[(3-{[(4- methylphenyl)sulfonyl]amino} quinoxalin-2-yl)amino]-4,5,6,7- tetrahydro-1-benzothiophene-3- carboxylate 90

2,5-dichloro-N-{3-[(2-morpholin- 4-ylphenyl)amino]quinoxalin- 2-yl}benzenesulfonamide 91

N-{4-[({3-[(3-methylphenyl) amino]quinoxalin-2-yl}amino) sulfonyl]phenyl}acetamide 92

4-chloro-N-{3-[(3-chloro-4- piperidin-1-ylphenyl)amino]- 6-methylquinoxalin-2- yl}benzenesulfonamide 93

3-nitro-N-[3-(quinolin-6- ylamino)quinoxalin-2- yl]benzenesulfonamide 94

butyl N-{[4-({3-[(phenylsulfonyl) amino]quinoxalin-2-yl}amino) phenyl]carbonyl}glycinate 95

4-nitro-N-(3-{[3-(trifluoromethyl) phenyl]amino}quinoxalin-2- yl)benzenesulfonamide 96

N-[4-({3-[(phenylsulfonyl) amino]quinoxalin-2-yl} amino)phenyl]acetamide 97

N-{3-[(3-{[(4-methylphenyl) sulfonyl]amino}quinoxalin-2- yl)amino]phenyl}acetamide 98

ethyl 3,3,3-trifluoro-2-hydroxy- 2-{4-[(3-{[(4-methylphenyl) sulfonyl]amino}quinoxalin-2-yl) amino]phenyl}propanoate 99

N-{3-[(4-{[(2,6- dimethylpyrimidin-4-yl)amino] sulfonyl}phenyl)amino] quinoxalin-2-yl}-3- nitrobenzenesulfonamide 100

4-chloro-N-{3-[(3,4- dimethylphenyl)amino]-6- methylquinoxalin-2-yl} benzenesulfonamide 101

4-chloro-N-(6-methyl-3-{[3- (methoxy)phenyl]amino} quinoxalin-2-yl) benzenesulfonamide 102

butyl 4-[(3-{[(4-chlorophenyl) sulfonyl]amino}-7- methylquinoxalin-2-yl)amino] benzoate 103

4-chloro-N-{3-[(3-chloro-4- methylphenyl)amino]quinoxalin- 2-yl}benzenesulfonamide 104

1-methylethyl 4-[(3-{[(4- chlorophenyl)sulfonyl]amino} quinoxalin-2-yl)amino] benzoate 105

N-{3-[(2,5-dimethylphenyl) amino]-6-nitroquinoxalin-2- yl}-4-methylbenzenesulfonamide 106

N-[3-(cyclohexylamino)-6- nitroquinoxalin-2-yl]-4- methylbenzenesulfonamide 107

N-{3-[(2,4-dimethylphenyl) amino]quinoxalin-2-yl}-4- methylbenzenesulfonamide 108

N-(3-{[4-(ethyloxy)phenyl] amino}-6-methylquinoxalin-2- yl)-4-methylbenzenesulfonamide 109

3-({3-[({4-[hydroxy(oxido) amino]phenyl}sulfonyl)amino] quinoxalin-2-yl}amino) benzoic acid 110

N-{[4-({3-[(phenylsulfonyl) amino]quinoxalin-2-yl}amino) phenyl]carbonyl}glycine 111

N-{3-[(3-{[(4-chlorophenyl) sulfonyl]amino}-7- methylquinoxalin-2-yl)amino] phenyl}acetamide 112

4-chloro-N-{3-[(3,5-dimethyl- 1H-pyrazol-4-yl)amino]-6- methylquinoxalin-2-yl} benzenesulfonamide 113

4-bromo-N-{3-[(4′- nitrobiphenyl-3-yl)amino] quinoxalin-2-yl} benzenesulfonamide 114

4-bromo-N-{3-[(2-chlorophenyl) amino]quinoxalin-2- yl}benzenesulfonamide 115

N-{3-[(4-butylphenyl)amino]- 6-methylquinoxalin-2-yl}-4- chlorobenzenesulfonamide 116

N-{4-[(3-{[(4-chlorophenyl) sulfonyl]amino}-7- methylquinoxalin-2-yl) amino]phenyl}acetamide 117

4-chloro-N-{6-methyl-3-[(2- oxo-2,3-dihydro-1H- benzimidazol-5-yl)amino] quinoxalin-2-yl} benzenesulfonamide 118

propyl 4-[(3-{[(4-chlorophenyl) sulfonyl]amino}-7- methylquinoxalin-2-yl)amino] benzoate 119

4-chloro-N-{3-[(4-fluorophenyl) amino]quinoxalin-2-yl} benzenesulfonamide 120

N-[4-({[3-(naphthalen-2- ylamino)quinoxalin-2-yl] amino}sulfonyl)phenyl] acetamide 121

4-bromo-N-(3-{[4- (phenylamino)phenyl] amino}quinoxalin-2-yl) benzenesulfonamide 122

2-hydroxy-4-({3- [(phenylsulfonyl)amino] quinoxalin-2- yl}amino)benzoic acid 123

N-(3-{[3-(aminosulfonyl) phenyl]amino}quinoxalin-2- yl)-4-methylbenzenesulfonamide 124

4-[(3-{[(3-nitrophenyl)sulfonyl] amino}quinoxalin-2- yl)amino]benzoic acid 125

N-(3-{[3-(butyloxy)phenyl] amino}quinoxalin-2-yl)-4- methylbenzenesulfonamide 126

N-{3-[(4-fluorophenyl)amino] quinoxalin-2-yl}-3- nitrobenzenesulfonamide 127

4-{[3-({[4-(acetylamino)phenyl] sulfonyl}amino)quinoxalin- 2-yl]amino}-2- hydroxybenzoic acid 128

N-[3-(naphthalen-1-ylamino) quinoxalin-2-yl]-4- nitrobenzenesulfonamide 129

4-[(3-{[(4-bromophenyl) sulfonyl]amino}quinoxalin-2- yl)amino]benzoic acid 130

N-{4-[({3-[(3-hydroxyphenyl) amino]quinoxalin-2-yl}amino) sulfonyl]phenyl}acetamide 131

3-[(3-{[(4-bromophenyl) sulfonyl]amino}quinoxalin-2- yl)amino]benzoic acid 132

4-bromo-N-(3-{[3- (butyloxy)phenyl]amino} quinoxalin-2-yl) benzenesulfonamide 133

4-bromo-N-(3-{[3- (trifluoromethyl)phenyl] amino}quinoxalin-2-yl) benzenesulfonamide 134

4-methyl-N-{3-[(4′-nitrobiphenyl- 3-yl)amino]quinoxalin-2-yl} benzenesulfonamide 135

4-chloro-N-{3-[(3-fluorophenyl) amino]quinoxalin-2-yl} benzenesulfonamide 136

N-{3-[(2-chlorophenyl)amino] quinoxalin-2-yl} benzenesulfonamide 137

4-bromo-N-[3-(quinolin-5- ylamino)quinoxalin-2- yl]benzenesulfonamide 138

N-{3-[(3-fluorophenyl)amino] quinoxalin-2-yl}-4- methylbenzenesulfonamide 139

N-{3-[(4-fluorophenyl)amino] quinoxalin-2-yl}-4- methylbenzenesulfonamide 140

3-nitro-N-(3-{[3- (trifluoromethyl)phenyl] amino}quinoxalin-2- yl)benzenesulfonamide 141

2-hydroxy-4-[(3-{[(3- nitrophenyl)sulfonyl]amino} quinoxalin-2-yl)amino] benzoic acid 142

N-{3-[(3-chlorophenyl)amino] quinoxalin-2-yl}-4- methylbenzenesulfonamide 143

N-[3-(1,3-benzodioxol-5-ylamino) quinoxalin-2-yl]-4- bromobenzenesulfonamide 144

N-{3-[(3-acetylphenyl)amino] quinoxalin-2-yl}-4- chlorobenzenesulfonamide 145

3-nitro-N-(3-{[4-(9H-xanthen- 9-yl)phenyl]amino}quinoxalin- 2-yl)benzenesulfonamide 146

4-chloro-N-{3-[(4′-nitrobiphenyl- 3-yl)amino]quinoxalin-2- yl}benzenesulfonamide 147

N-[3-(2,1,3-benzothiadiazol-5- ylamino)quinoxalin-2- yl]-4-tolylsulfonamide 148

N-{3-[(2-methyl-1,3-dioxo-2,3- dihydro-1H-isoindol-5-yl) amino]quinoxalin-2- yl}benzenesulfonamide 149

4-methyl-N-[3-(quinolin-5- ylamino)quinoxalin-2-yl] benzenesulfonamide 150

4-methyl-N-{3-[(1-oxo-1,3- dihydro-2-benzofuran-5-yl) amino]quinoxalin-2-yl} benzenesulfonamide 151

4-chloro-N-{3-[(2-chlorophenyl) amino]quinoxalin-2-yl] benzenesulfonamide 152

2-hydroxy-5-[(3-{[(4- methylphenyl)sulfonyl]amino} quinoxalin-2- yl)amino]benzoic acid 153

N-(3-{[3,5-bis(1,1- dimethylethyl)-4- hydroxyphenyl]amino} quinoxalin-2-yl) benzenesulfonamide 154

N-[3-({2- [(trifluoromethyl) thio]phenyl} amino)quinoxalin-2-yl] benzenesulfonamide 155

N-{4-[({3-[(4- hydroxyphenyl)amino] quinoxalin-2-yl}amino) sulfonyl]phenyl}acetamide 156

N-[3-(1,3-benzodioxol- 5-ylamino)quinoxalin- 2-yl]-4- methylbenzenesulfonamide 157

N-(3-{[2,5- bis(methoxy)phenyl] amino}quinoxalin-2-yl) benzenesulfonamide 158

N-{3-[(2,4- dichlorophenyl)amino] quinoxalin-2-yl} benzenesulfonamide 159

N-[4-({[3-(2,3-dihydro-1,4- benzodioxin-6-ylamino) quinoxalin-2-yl]amino}sulfonyl) phenyl]acetamide 160

4-chloro-N-{3-[(3,4- dimethylphenyl)amino] quinoxalin-2-yl} benzenesulfonamide 161

N-(3-{[2,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-3- nitrobenzenesulfonamide 162

4-bromo-N-{3-[(3,4- dimethylphenyl)amino] quinoxalin-2-yl} benzenesulfonamide 163

5-{[3-({[4-(acetylamino)phenyl] sulfonyl}amino)quinoxalin-2- yl]amino}-2- hydroxybenzoic acid 164

N-(3-{[2,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl)- 4-chlorobenzenesulfonamide 165

N-(3-{[2,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-4- methylbenzenesulfonamide 166

N-{3-[(2,4-dichlorophenyl) amino]quinoxalin-2-yl}-4- methylbenzenesulfonamide 167

4-bromo-N-{3-[(3-fluorophenyl) amino]quinoxalin-2-yl} benzenesulfonamide 168

4-{[3-({[4-(acetylamino) phenyl]sulfonyl}amino) quinoxalin-2-yl]amino} benzoic acid 169

N-{3-[(2-fluorophenyl) amino]quinoxalin-2-yl}-4- methylbenzenesulfonamide 170

N-[3-(2,3-dihydro-1,4- benzodioxin-6-ylamino) quinoxalin-2-yl]-4- methylbenzenesulfonamide 171

N-{3-[(3,4-dimethylphenyl) amino]quinoxalin-2-yl} benzenesulfonamide 172

4-methyl-N-(3-{[3- (trifluoromethyl)phenyl] amino}quinoxalin-2-yl) benzenesulfonamide 173

5-[(3-{[(4-chlorophenyl) sulfonyl]amino}quinoxalin- 2-yl)amino]-2- hydroxybenzoic acid 174

3-nitro-N-{3-[(1-oxo-1,3- dihydro-2-benzofuran-5-yl) amino]quinoxalin-2-yl} benzenesulfonamide 175

N-{4-[({3-[(2-bromo-4- methylphenyl)amino] quinoxalin-2-yl}amino) sulfonyl]phenyl}acetamide 176

N-{3-[(2-fluorophenyl)amino] quinoxalin-2-yl}-4- nitrobenzenesulfonamide 177

N-{3-[(2-methyl-1,3-dioxo- 2,3-dihydro-1H-isoindol-5-yl) amino]quinoxalin-2-yl}-3- nitrobenzenesulfonamide 178

4-chloro-N-{3-[(1-oxo-1,3- dihydro-2-benzofuran-5-yl) amino]quinoxalin-2- yl}benzenesulfonamide 179

N-{3-[(1-oxo-1,3-dihydro-2- benzofuran-5-yl)amino] quinoxalin-2-yl} benzenesulfonamide 180

N-{3-[(2-fluorophenyl)amino] quinoxalin-2-yl}-3- nitrobenzenesulfonamide 181

N-[2-(butyloxy)-2-hydroxyethyl]- 4-({3-[(phenylsulfonyl)amino] quinoxalin-2-yl}amino) benzamide 182

3-nitro-N-(3-{[4- (phenylamino)phenyl]amino} quinoxalin-2- yl)benzenesulfonamide 183

4-bromo-N-{3-[(4-fluorophenyl) amino]quinoxalin-2-yl} benzenesulfonamide 184

4-methyl-N-[3-({2- [(trifluoromethyl)thio] phenyl}amino) quinoxalin-2-yl] benzenesulfonamide 185

N-[4-({3-[2-(methoxy)phenyl]- 2,3-dihydro-1H-imidazo[4,5-b] quinoxalin-1-yl}sulfonyl) phenyl]acetamide 186

4-(3-{[4-(acetylamino)phenyl] sulfonyl}-2,3-dihydro-1H- imidazo[4,5-b]quinoxalin-1- yl)benzoic acid 187

1-naphthalen-2-yl-3-[(3- nitrophenyl)sulfonyl]-2,3- dihydro-1H-imidazo[4,5- b]quinoxaline 188

N-[4-({3-[4-(methoxy)phenyl]- 2,3-dihydro-1H-imidazo[4,5- b]quinoxalin-1-yl}sulfonyl) phenyl]acetamide 189

1-(3-methylphenyl)-3-[(4- methylphenyl)sulfonyl]-2,3- dihydro-1H-imidazo [4,5-b]quinoxaline 190

N-(4-{[3-(4-methylphenyl)-2,3- dihydro-1H-imidazo[4,5-b] quinoxalin-1-yl]sulfonyl} phenyl)acetamide 191

N-{4-[(3-phenyl-2,3-dihydro-1H- imidazo[4,5-b]quinoxalin-1-yl) sulfonyl]phenyl}acetamide 192

N-(4-{[3-(3-methylphenyl)- 2,3-dihydro-1H-imidazo[4,5-b] quinoxalin-1-yl]sulfonyl} phenyl)acetamide 193

1-[4-(methoxy)phenyl]-3-[(4- methylphenyl)sulfonyl]-2,3- dihydro-1H-imidazo[4,5-b] quinoxaline 194

N-(4-{[3-(2-methylphenyl)- 2,3-dihydro-1H-imidazo [4,5-b]quinoxalin-1-yl]sulfonyl} phenyl)acetamide 195

1-(3-methylphenyl)-3-[(3- nitrophenyl)sulfonyl]-2,3- dihydro-1H-imidazo[4,5-b] quinoxaline 196

1-(4-methylphenyl)-3-[(3- nitrophenyl)sulfonyl]-2,3- dihydro-1H-imidazo[4,5-b] quinoxaline 197

N-{3-[(4-methylphenyl)amino] quinoxalin-2-yl}-3-(1H-tetrazol- 1-yl)benzenesulfonamide 198

N-(3-{[2-(ethyloxy)phenyl] amino}quinoxalin-2-yl)-4- methylbenzenesulfonamide 199

N-{4-[({3-[(4-ethylphenyl) amino]quinoxalin-2-yl}amino) sulfonyl]phenyl}acetamide 200

4-bromo-N-(3-{[3-(methoxy) phenyl]amino}quinoxalin-2- yl)benzenesulfonamide 201

N-(4-{[(3-{[4-(ethyloxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl} phenyl)acetamide 202

N-{4-[({3-[(2-ethylphenyl) amino]quinoxalin-2-yl}amino) sulfonyl]phenyl}acetamide 203

N-(4-{[(3-{[2-(ethyloxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl) acetamide 204

N-{3-[(4-nitrophenyl)amino] quinoxalin-2-yl} benzenesulfonamide 205

4-(ethyloxy)-N-(3-{[4-(methoxy) phenyl]amino}quinoxalin-2- yl)benzenesulfonamide 206

methyl N-acetyl-N-[4-({3- [(phenylsulfonyl)amino] quinoxalin-2-yl}amino) phenyl]-beta-alaninate 207

methyl N-acetyl-N-{4-[(3-{[(4- chlorophenyl)sulfonyl]amino} quinoxalin-2-yl)amino]phenyl}- beta-alaninate 208

N-{3-[(3-chloro-5-methylphenyl) amino]quinoxalin-2-yl}- 4-methylbenzenesulfonamide 209

N-{3-[(3-acetylphenyl)amino] quinoxalin-2-yl}-3- nitrobenzenesulfonamide 210

4-{[3-({[4-(acetylamino)phenyl] sulfonyl}amino)quinoxalin-2- yl]amino}-N-[4-(methoxy) phenyl]benzamide 211

2-hydroxy-5-({3- [(phenylsulfonyl)amino] quinoxalin-2-yl}amino) benzoic acid 212

N-[3-(2,3-dihydro-1,4- benzodioxin-6-ylamino) quinoxalin-2-yl]-3- nitrobenzenesulfonamide 213

N-[4-(methoxy)phenyl]- 4-[(3-{[(4-nitrophenyl) sulfonyl]amino}quinoxalin-2- yl)amino]benzamide 214

4-chloro-N-{3-[(2-oxo-2,3- dihydro-1H-benzimidazol-5-yl) amino]quinoxalin-2- yl}benzenesulfonamide 215

4-methyl-N-{3- [methyl(phenylmethyl) amino]quinoxalin-2- yl}benzenesulfonamide 216

N-[3-(3,4- dihydroisoquinolin-2(1H)- yl)quinoxalin-2-yl]-2- methylbenzenesulfonamide 217

N-[4-({[3-(2,1,3-benzothiadiazol- 5-ylamino)quinoxalin-2-yl] amino}sulfonyl)phenyl] acetamide 218

4-bromo-N-{3-[(4- phenylquinolin-8-yl)amino] quinoxalin-2-yl} benzenesulfonamide 219

4-methyl-N-{3-[(4- phenylquinolin-8-yl)amino] quinoxalin-2-yl} benzenesulfonamide 220

1-[(4-chlorophenyl) sulfonyl]-3-[4-(pyrrolidin- 1-ylsulfonyl)phenyl]-2,3- dihydro-1H-imidazo [4,5-b]quinoxaline 221

1-(4-morpholin-4-ylphenyl)-3- (phenylsulfonyl)-2,3-dihydro- 1H-imidazo[4,5-b]quinoxaline 222

methyl 4,5-dimethyl-2-({3- [(phenylsulfonyl)amino] quinoxalin-2-yl}amino) thiophene-3-carboxylate 223

ethyl 6-methyl-2-[(3-{[(2- methylphenyl)sulfonyl] amino}quinoxalin-2-yl) amino]-4,5,6,7-tetrahydro- 1-benzothiophene-3- carboxylate 224

ethyl 2-{[3-({[4- (acetylamino)phenyl] sulfonyl}amino)quinoxalin- 2-yl]amino}-6-phenyl- 4,5,6,7-tetrahydro-1- benzothiophene-3- carboxylate 225

ethyl 6-methyl-2-[(3-{[(4- methylphenyl)sulfonyl] amino}quinoxalin-2-yl) amino]-4,5,6,7-tetrahydro- 1-benzothiophene-3- carboxylate 226

propyl 4-[(3-{[(4- chlorophenyl)sulfonyl] amino}quinoxalin-2- yl)amino]benzoate 227

N-{3-[(4-butylphenyl) amino]quinoxalin-2-yl}-4- chlorobenzenesulfonamide 228

N-{3-[(2- chlorophenyl)amino] quinoxalin-2-yl}-4- methylbenzenesulfonamide 229

N-{3-[(2,3- dimethylphenyl)amino] quinoxalin-2-yl}-4- methylbenzenesulfonamide 230

N-{3-[(3,4- dimethylphenyl)amino] quinoxalin-2-yl}-3- nitrobenzenesulfonamide 231

N-{4-[({3-[(2,3- dimethylphenyl)amino] quinoxalin-2-yl}amino) sulfonyl]phenyl}acetamide 232

4-chloro-N-{3-[(2,3- dimethylphenyl)amino] quinoxalin-2-yl} benzenesulfonamide 233

3-nitro-N-(3-{[3,4,5- tris(methoxy)phenyl] amino}quinoxalin-2- yl)benzenesulfonamide 234

4-chloro-N-{3-[(2,4- dichlorophenyl)amino] quinoxalin-2-yl} benzenesulfonamide 235

N-{3-[(2,3- dimethylphenyl)amino] quinoxalin-2-yl}-3- nitrobenzenesulfonamide 236

N-{4-[({3-[(3,4- dimethylphenyl)amino] quinoxalin-2- yl}amino)sulfonyl] phenyl}acetamide 237

ethyl 2-[(3-{[(4- chlorophenyl)sulfonyl] amino}quinoxalin-2- yl)amino]-5,6-dihydro-4H- cyclopenta[b]thiophene- 3-carboxylate 238

4-chloro-N-(3-{[4-chloro- 3-(morpholin-4- ylsulfonyl)phenyl]amino} quinoxalin-2-yl) benzenesulfonamide 239

ethyl 2-[(3-{[(2- methylphenyl)sulfonyl] amino}quinoxalin-2- yl)amino]-4,5,6,7- tetrahydro-1- benzothiophene-3- carboxylate 240

4-bromo-N-{3-[(2,4- dichlorophenyl)amino] quinoxalin-2- yl}benzenesulfonamide 241

ethyl 5-ethyl-2-[(3-{[(3- nitrophenyl)sulfonyl] amino}quinoxalin-2-yl) amino]thiophene-3- carboxylate 242

N-(3-{[3-(morpholin-4- ylsulfonyl)phenyl] amino}quinoxalin-2- yl)benzenesulfonamide 243

ethyl 2-[(3-{[(4- bromophenyl)sulfonyl] amino}quinoxalin-2-yl) amino]-4,5,6,7-tetrahydro- 1-benzothiophene-3- carboxylate 244

4-methyl-N-(3-{[3- (piperidin-1-ylsulfonyl) phenyl]amino}quinoxalin- 2-yl)benzenesulfonamide 245

4-chloro-N-(3-{[4- (morpholin-4-ylsulfonyl) phenyl]amino}quinoxalin- 2-yl)benzenesulfonamide 246

4-chloro-N-(3-{[3- (morpholin-4-ylsulfonyl) phenyl]amino}quinoxalin- 2-yl)benzenesulfonamide 247

4-methyl-N-[3-(quinolin- 6-ylamino)quinoxalin- 2-yl]benzenesulfonamide 248

N-(3-{[3-(piperidin-1- ylsulfonyl)phenyl] amino}quinoxalin-2- yl)benzenesulfonamide 249

N-(3-{[4- (phenylamino)phenyl] amino}quinoxalin-2- yl)benzenesulfonamide 250

N-(3-{[2,5-bis(methoxy) phenyl]amino} quinoxalin-2-yl)-4- bromobenzenesulfonamide 251

ethyl 2-[(3-{[(3- nitrophenyl)sulfonyl] amino}quinoxalin-2-yl) amino]-5,6-dihydro-4H- cyclopenta[b]thiophene- 3-carboxylate 252

N-{3-[(4′-nitrobiphenyl- 4-yl)amino]quinoxalin- 2-yl}benzenesulfonamide 253

ethyl 2-[(3-{[(3- nitrophenyl)sulfonyl] amino}quinoxalin-2-yl) amino]-4,5,6,7-tetrahydro- 1-benzothiophene-3- carboxylate 254

N-(3-{[4-chloro-3- (morpholin-4- ylsulfonyl)phenyl] amino}quinoxalin-2- yl)benzenesulfonamide 255

ethyl 5-ethyl-2-({3- [(phenylsulfonyl)amino] quinoxalin-2-yl}amino) thiophene-3-carboxylate 256

N-[4-({[3-(quinolin-6- ylamino)quinoxalin-2- yl]amino}sulfonyl) phenyl]acetamide 257

ethyl 2-[(3-{[(2- methylphenyl)sulfonyl] amino}quinoxalin-2- yl)amino]-5,6-dihydro- 4H-cyclopenta[b] thiophene-3-carboxylate 258

3,4-dichloro-N-[3- (naphthalen-1-ylamino) quinoxalin-2-yl] benzenesulfonamide 259

ethyl 2-{[3-({[4- (acetylamino)-3,5- dibromophenyl]sulfonyl} amino)quinoxalin-2-yl] amino}-4,5,6,7-tetrahydro- 1-benzothiophene-3- carboxylate 260

ethyl 2-[(3-{[(2-chloro-5- nitrophenyl)sulfonyl] amino}quinoxalin-2-yl) amino]-4,5,6,7-tetrahydro- 1-benzothiophene-3- carboxylate 261

N-{3-[(3-fluorophenyl) amino]quinoxalin-2- yl}benzenesulfonamide 262

N-(3-{[4-(morpholin-4- ylsulfonyl)phenyl]amino} quinoxalin-2-yl) benzenesulfonamide 263

ethyl 2-{[3-({[4- (acetylamino)phenyl] sulfonyl}amino) quinoxalin-2-yl]amino}- 4,5,6,7-tetrahydro-1- benzothiophene-3- carboxylate 264

ethyl 2-[(3-{[(4- chlorophenyl)sulfonyl] amino}quinoxalin-2-yl) amino]-5-ethylthiophene- 3-carboxylate 265

N,N-diethyl-4-[(3-{[(4- methylphenyl)sulfonyl] amino}quinoxalin-2- yl)amino] benzenesulfonamide 266

ethyl 2-{[3-({[4- (acetylamino)phenyl] sulfonyl}amino) quinoxalin-2-yl]amino}- 5-ethylthiophene-3- carboxylate 267

ethyl 2-[(3-{[(4- chlorophenyl)sulfonyl] amino}quinoxalin-2-yl) amino]-4,5,6,7-tetrahydro- 1-benzothiophene-3- carboxylate 268

ethyl 2-({3- [(phenylsulfonyl)amino] quinoxalin-2-yl}amino)- 4,5,6,7-tetrahydro-1- benzothiophene-3- carboxylate 269

N-[4-(methoxy)phenyl]-4- [(3-{[(3-nitrophenyl) sulfonyl]amino}quinoxalin- 2-yl)amino]benzamide 270

N-{3-({4-[(4-aminophenyl) oxy]phenyl}amino) quinoxalin-2-yl]-4- chlorobenzenesulfonamide 271

N-[4-({[3-({4-[(4- aminophenyl)oxy]phenyl} amino)quinoxalin-2-yl] amino}sulfonyl)phenyl] acetamide 272

(2E)-3-{3-[(3-{[(4- methylphenyl)sulfonyl] amino}quinoxalin-2-yl) amino]phenyl} prop-2-enoic acid 273

N-{3-[(9-ethyl-9H- carbazol-3-yl)amino] quinoxalin-2-yl}-3- nitrobenzenesulfonamide 274

N-[3-({4-[(4- aminophenyl)oxy]phenyl} amino)quinoxalin-2- yl]benzenesulfonamide 275

4-bromo-N-{3-[(9-ethyl- 9H-carbazol-3-yl) amino]quinoxalin-2-yl} benzenesulfonamide 276

N-{3-[(9-ethyl-9H- carbazol-3-yl)amino] quinoxalin-2-yl} benzenesulfonamide 277

N-{3-[(2-iodophenyl) amino]quinoxalin-2- yl}benzenesulfonamide 278

N-{3-[(1- phenylethyl)amino] quinoxalin-2- yl}benzenesulfonamide 279

4-bromo-N-{3-[(4- bromophenyl)amino] quinoxalin-2- yl}benzenesulfonamide 280

4-bromo-N-{3-[(4- chlorophenyl)amino] quinoxalin-2- yl}benzenesulfonamide 281

4-bromo-N-[3-(naphthalen- 2-ylamino)quinoxalin-2- yl]benzenesulfonamide 282

N-{3-[(2,3- dimethylphenyl)amino]-6- methylquinoxalin-2-yl}-4- methylbenzenesulfonamide 283

4-chloro-N-{3-[(2- iodophenyl)amino] quinoxalin-2- yl}benzenesulfonamide 284

N-(3-{[4-(octyloxy)phenyl] amino}quinoxalin-2- yl)benzenesulfonamide 285

N-[3-(2,1,3- benzothiadiazol-5-ylamino) quinoxalin-2-yl]-3- nitrobenzenesulfonamide 286

N-{3-[(2-bromo-4- methylphenyl)amino] quinoxalin-2- yl}benzenesulfonamide 287

N-[3-({4-[(3-aminophenyl) sulfonyl]phenyl}amino) quinoxalin-2-yl]-4- chlorobenzenesulfonamide 288

N-[3-({2-[(difluoromethyl) oxy]phenyl}amino) quinoxalin-2-yl]-3- nitrobenzenesulfonamide 289

8-[(3-{[(4- methylphenyl)sulfonyl] amino}quinoxalin-2- yl)amino]quinoline-2- carboxylic acid 290

ethyl 3,3,3-trifluoro-2- hydroxy-2-{4-[(3-{[(3- nitrophenyl)sulfonyl] amino}quinoxalin-2-yl) amino]phenyl}propanoate 291

N-[3-(quinolin-6- ylamino)quinoxalin-2- yl]benzenesulfonamide 292

4-{[3-({[4-(acetylamino) phenyl]sulfonyl}amino) quinoxalin-2-yl]amino} phenyl thiocyanate 293

1-[3-({[4-(acetylamino) phenyl]sulfonyl}amino) quinoxalin-2-yl]-4- methylpyridinium 294

N-{3-[(2-chlorophenyl) amino]quinoxalin-2-yl}-3- nitrobenzenesulfonamide 295

4-methyl-N-[3- (phenylamino)quinoxalin- 2-yl]benzenesulfonamide 296

4-methyl-N-{3-[(2- methylphenyl)amino] quinoxalin-2- yl}benzenesulfonamide 297

4-methyl-N-{3-[(4- methylphenyl)amino] quinoxalin-2- yl}benzenesulfonamide 298

N-{3-[(4- chlorophenyl)amino] quinoxalin-2-yl}-4- methylbenzenesulfonamide 299

4-methyl-N-[3- (naphthalen-2-ylamino) quinoxalin-2-yl] benzenesulfonamide 300

N-{4-[({3-[(4- bromophenyl)amino] quinoxalin-2-yl}amino) sulfonyl]phenyl} acetamide 301

N-{4-[({3-[(2- methylphenyl)amino] quinoxalin-2-yl}amino) sulfonyl]phenyl} acetamide 302

N-{3-[bis (phenylmethyl)amino] quinoxalin-2-yl} benzenesulfonamide 303

4-[(3-{[(4- methylphenyl)sulfonyl] amino}quinoxalin-2- yl)amino]benzoic acid 304

2-hydroxy-4-[(3-{[(4- methylphenyl)sulfonyl] amino}quinoxalin-2- yl)amino]benzoic acid 305

4-bromo-N-(3-{[2- (methoxy)phenyl]amino} quinoxalin-2- yl)benzenesulfonamide 306

N-{3-[(3-hydroxyphenyl) amino]quinoxalin-2- yl}benzenesulfonamide 307

N-[3-(naphthalen-1- ylamino)quinoxalin-2- yl]benzenesulfonamide 308

3-methyl-1-(3-{[(4- methylphenyl)sulfonyl] amino}quinoxalin-2- yl)pyridinium 309

N-(3-{[3-{[(4- chlorophenyl)sulfonyl] amino}-7-(methoxy) quinoxalin-2-yl] amino}phenyl)acetamide 310

N-{3-[(3-{[(4- chlorophenyl)sulfonyl] amino}quinoxalin-2-yl) amino]phenyl}acetamide 311

N-{3-[(4-bromophenyl) amino]quinoxalin-2-yl}-4- chlorobenzenesulfonamide 312

N-{3-[(2,4- dimethylphenyl)amino]-6- methylquinoxalin-2-yl}-4- methylbenzenesulfonamide 313

N-{3-[(3,4- dimethylphenyl)amino] quinoxalin-2-yl}-4- methylbenzenesulfonamide 314

N-{3-[(2,5- dimethylphenyl)amino]-6- methylquinoxalin-2-yl}-4- methylbenzenesulfonamide 315

ethyl 4-[(3-{[(4- chlorophenyl)sulfonyl] amino}quinoxalin-2- yl)amino]benzoate 316

4-chloro-N-{3-[(4- ethylphenyl)amino] quinoxalin-2- yl}benzenesulfonamide 317

4-chloro-N-(6-methyl-3- {[4-(methoxy)phenyl] amino}quinoxalin-2- yl)benzenesulfonamide 318

4-chloro-N-{3-[(4- chlorophenyl)amino]- 6-methylquinoxalin-2- yl}benzenesulfonamide 319

N-(3-{[4-chloro-2,5- bis(methoxy)phenyl] amino}quinoxalin-2- yl)benzenesulfonamide 320

N-(3-{[3,5- bis(methoxy)phenyl] amino}quinoxalin-2- yl)benzenesulfonamide 321

N-(3-{[3,5-bis(methoxy) phenyl]amino} quinoxalin-2-yl)-4- methylbenzenesulfonamide 322

N-(3-{[3,5-bis(methoxy) phenyl]amino} quinoxalin-2-yl)-3- nitrobenzenesulfonamide 323

N-(3-{[2-methyl-5- (methoxy)phenyl] amino}quinoxalin-2- yl)benzenesulfonamide 324

N-[3-(2-Chloro-5- methoxy-phenylamino)- quinoxalin-2-yl]- benzensulfonamide 325

3-amino-N-(3-{[3,5- bis(methoxy)phenyl] amino}quinoxalin-2- yl)benzenesulfonamide 326

N-(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)-4- chlorobenzenesulfonamide 327

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)acetamide 328

N-(3-{[4-chloro-3- (methoxy)phenyl] amino}quinoxalin-2-yl) benzenesulfonamide 329

N-(3-{[4-fluoro-3-(methoxy) phenyl]amino}quinoxalin- 2-yl)benzenesulfonamide 330

3-amino-N-(3-{[2,5- bis(methoxy)phenyl] amino}quinoxalin-2- yl)benzenesulfonamide 331

N-(3-{[3,5-bis(methoxy) phenyl]amino} quinoxalin-2-yl)-4- bromobenzenesulfonamide 332

N-(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)-3- nitrobenzenesulfonamide 333

3-amino-N-(3-{[2-chloro- 5-(methoxy)phenyl] amino}quinoxalin-2- yl)benzenesulfonamide 334

N-(3-{[(3-{[3,5- bis(methoxy)phenyl] amino}quinoxalin-2- yl)amino]sulfonyl} phenyl)-N-2-,N-2- dimethylglycinamide 335

N-(3-{[2,5-bis(methoxy) phenyl]amino}-7- methylquinoxalin-2- yl)benzenesulfonamide 336

N-(3-{[2,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)-4-(methoxy) benzenesulfonamide 337

N-(3-{[2,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)-3- bromobenzenesulfonamide 338

N-(3-{[2,5-bis(methoxy) phenyl]amino} quinoxalin-2-yl)-3- fluorobenzenesulfonamide 339

N-(3-{[3,5- bis(methoxy)phenyl] amino}quinoxalin-2-yl)-2- fluorobenzenesulfonamide 340

N-(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)-4-(methoxy) benzenesulfonamide 341

N-(3-{[3,5-bis(methoxy) phenyl]amino} quinoxalin-2-yl)-3- bromobenzenesulfonamide 342

N-(3-{[(3-{[3,5-bis (methoxy)phenyl] amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-1- methylpiperidine-4- carboxamide 343

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-3- piperidin-1-ylpropanamide 344

N-(3-{[(3-{[3,5- bis(methoxy)phenyl] amino}quinoxalin-2- yl)amino]sulfonyl} phenyl)-4-(dimethylamino) butanamide 345

N-(3-{[3,5- bis(methoxy)phenyl] amino}quinoxalin-2- yl)-3-(hydroxyamino) benzenesulfonamide 346

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2- morpholin-4-ylacetamide 347

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}-4-methylphenyl)- N-2-methylglycinamide 348

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}-4-methylphenyl)- L-alaninamide 349

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}-4-methylphenyl)- 2-methylalaninamide 350

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}-4-methylphenyl)- N-2-,N-2- dimethylglycinamide 351

N-(3-{[(3-{[3,5- bis(methoxy)phenyl] amino}quinoxalin-2- yl)amino]sulfonyl} phenyl)-D-alaninamide 352

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- methylglycinamide 353

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}-4-methylphenyl)- D-alaninamide 354

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- methylglycinamide 355

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-L- alaninamide 356

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-D- alaninamide 357

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2- methylalaninamide 358

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2- methylalaninamide 359

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}-4- methylphenyl)-N-2-,N-2- dimethylglycinamide 360

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-[2- (dimethylamino)ethyl]- N-2-methylglycinamide 361

(2S)-2-amino-N-(3-{[(3- {[2-chloro-5-(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl} phenyl)butanamide 362

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-[2- (dimethylamino)ethyl]-N- 2-methylglycinamide 363

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-,N-2- dimethylglycinamide 364

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- methyl-L-alaninamide 365

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl) glycinamide 366

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl) glycinamide 367

N-(2-chloro-5-{[(3-{[2- chloro-5-(methoxy)phenyl] amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)- N-2-methylglycinamide 368

2-(dimethylamino)- N-(3-(N-(3-(3-(2- (dimethylamino)acetamido)- 5-methoxyphenylamino) quinoxalin-2-yl)sulfamoyl) phenyl)acetamide 369

N-(3-{[(3-{[2-acetyl-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-,N-2- dimethylglycinamide 370

N-(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)-3- (formylamino) benzenesulfonamide 371

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- ethylglycinamide 372

N-(5-{[(3-{[3,5- bis(methoxy)phenyl] amino}quinoxalin-2- yl)amino]sulfonyl}-2- methylphenyl)glycinamide 373

2-azetidin-1-yl-N-(3-{[(3- {[2-chloro-5-(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl} phenyl)acetamide 374

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-L- prolinamide 375

N-(3-{[(3-{[2-bromo-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- methylglycinamide 376

N-2-,N-2-dimethyl-N-(3- {[(3-{[6-(methoxy) quinolin-8-yl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl) glycinamide 377

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-L- alaninamide 378

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- methyl-D-alaninamide 379

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-L- prolinamide 380

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-D- serinamide 381

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl) azetidine-3-carboxamide 382

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-,2- dimethylalaninamide 383

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- methyl-D-alaninamide 384

N-(3-{[(3-{[2-bromo-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-, N-2-dimethylglycinamide 385

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- propylglycinamide 386

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- methyl-L-alaninamide 387

N-(5-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}-2-methylphenyl)- beta-alaninamide 388

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl) piperidine-3-carboxamide 389

N-(3-{[(3-{[3,5- bis(methoxy)phenyl] amino}quinoxalin-2- yl)amino]sulfonyl} phenyl)-2-(4-methyl-1,4- diazepan-1-yl)acetamide 390

(2S)-2-amino-N-(3-{[(3- {[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl) amino]sulfonyl} phenyl)butanamide 391

N-(3-{[(3-{[3,5-bis (methoxy)phenyl] amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)- N-2-(2-hydroxypropyl) glycinamide 392

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-(2- fluoroethyl)glycinamide 393

3-amino-N-(2-{[3,5-bis (methoxy)phenyl]amino} pyrido[2,3-b]pyrazin-3-yl) benzenesulfonamide 394

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-[(2- methylpropyl)oxy] glycinamide 395

1-amino-N-(3-{[(3-{[2- chloro-5-(methoxy)phenyl] amino}quinoxalin-2-yl) amino]sulfonyl}phenyl) cyclopropanecarboxamide 396

N-(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)-3-(formylamino) benzenesulfonamide 397

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- (cyclopropylmethyl) glycinamide 398

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-D- prolinamide 399

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2-[3- (dimethylamino)azetidin- 1-yl]acetamide 400

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-D- prolinamide 401

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl) piperidine-2-carboxamide 402

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl) morpholine-4-carboxamide 403

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2- pyrrolidin-1-ylacetamide 404

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-6-,N-6- dimethyl-L-lysinamide 405

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- ethyl-N-2- methylglycinamide 406

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2-(1H- imidazol-4-yl)acetamide 407

1-amino-N-(3-{[(3-{[2- chloro-5-(methoxy)phenyl] amino}quinoxalin-2- yl)amino]sulfonyl}phenyl) cyclopentanecarboxamide 408

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-(2- methylpropyl)glycinamide 409

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- ethyl-N-2- methylglycinamide 410

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-1-(1H- imidazol-4-ylmethyl) azetidine-3-carboxamide 411

N-(5-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}-2-methylphenyl)- N-2-,N-2- dimethylglycinamide 412

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-1- ethylazetidine-3- carboxamide 413

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- methyl-N-2-(1- methylpyrrolidin-3- yl)glycinamide 414

N-(3-{[(2-{[3,5-bis (methoxy)phenyl]amino} pyrido[2,3-b]pyrazin-3- yl)amino]sulfonyl} phenyl)-N-2-[2- (dimethylamino)ethyl]-N- 2-methylglycinamide 415

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2-[(3S)- 3-hydroxypyrrolidin- 1-yl]acetamide 416

1-amino-N-(3-{[(3-{[3,5- bis(methoxy)phenyl] amino}quinoxalin-2-yl) amino]sulfonyl}phenyl) cyclobutanecarboxamide 417

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- butylglycinamide 418

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2-(3- piperidin-1-ylazetidin-1- yl)acetamide 419

3-[(aminocarbonyl)amino]- N-(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)benzenesulfonamide 420

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-1- hydroxycyclopropanecarboxamide 421

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- (2,2-dimethylhydrazino) acetamide 422

N-(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)-3-[({[2-(dimethylamino) ethyl]amino}carbonyl)amino] benzenesulfonamide 423

N-(3-{[(3-{[3-fluoro-5-(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-N-2- methylglycinamide 424

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-2- hydroxyacetamide 425

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl) pyridazine-4-carboxamide 426

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-N-2- (1-methylethyl)glycinamide 427

1-amino-N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl) cyclopentanecarboxamide 428

1-amino-N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl) cyclopropanecarboxamide 429

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-2-[3- (dimethylamino) pyrrolidin-1-yl]acetamide 430

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl}phenyl)- N-2-[2-(dimethylamino)ethyl] glycinamide 431

2-(dimethylamino)ethyl(3- {[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl} phenyl)carbamate 432

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-1- (cyclopropylmethyl) azetidine-3-carboxamide 433

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- (1,1-dimethylethyl) glycinamide 434

N-2-methyl-N-(3-{[(3-{[3- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl) glycinamide 435

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-1H- imidazole-2-carboxamide 436

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl) isoxazole-5-carboxamide 437

N-(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-(2,2,2- trifluoroethyl)glycinamide 438

3-amino-N-(3-{[2-methyl- 5-(methoxy)phenyl]amino} quinoxalin-2- yl)benzenesulfonamide 439

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-3- oxocyclopentanecarboxamide 440

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl}phenyl)-6- hydroxypyridine-2-carboxamide 441

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N-2- (3-fluoro-4-hydroxyphenyl) glycinamide 442

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-1- (furan-2-ylmethyl)azetidine- 3-carboxamide 443

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl) pyrimidine-5-carboxamide 444

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-1H- pyrrole-2-carboxamide 445

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl}phenyl)- N-2-methyl-N-2-(1- methylethyl)glycinamide 446

N-(3-{[(3-{[3-fluoro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-,N-2- dimethylglycinamide 447

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-1H- imidazole-4-carboxamide 448

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-,N-2- diethylglycinamide 449

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2-(3- methylisoxazol-5-yl) acetamide 450

N-2-,N-2-dimethyl-N-(3- {[(3-{[2-methyl-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl) glycinamide 451

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl}phenyl)- N-2-[(3-hydroxyphenyl)methyl] glycinamide 452

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl}phenyl)- 1-methyl-1H-pyrrole-2- carboxamide 453

4-amino-N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)tetrahydro- 2H-pyran-4-carboxamide 454

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)- 2-[4-(methylamino)piperidin- 1-yl]acetamide 455

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl}phenyl)-2- piperidin-1-ylacetamide 456

N-(4-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl}phenyl)- N-2-,N-2-dimethylglycinamide 457

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl}phenyl)- 1-methyl-L-prolinamide 458

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl}phenyl) thiophene-3-carboxamide 459

3-amino-N-{3-[(2-chloro-5- hydroxyphenyl)amino] quinoxalin-2-yl} benzenesulfonamide 460

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl}phenyl)-1- (cyclopropylcarbonyl) azetidine-3-carboxamide 461

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl}phenyl)- 2-(4-methylpiperazin-1-yl) acetamide 462

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino(quinoxalin- 2-yl)amino]sulfonyl}phenyl)-1- (phenylmethyl)azetidine-3- carboxamide 463

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- y])amino]sulfonyl}phenyl)-2- chloropyridine-3-carboxamide 464

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl}phenyl)-2- pyridin-4-ylacetamide 465

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-methyl-N-2-prop-2-en- 1-ylglycinamide 466

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N-2- (phenylmethyl)glycinamide 467

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- (methoxy)acetamide 468

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl}phenyl)- 1-propanoylazetidine-3- carboxamide 469

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl) amino]sulfonyl}phenyl) pyridine-3-carboxamide 470

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-[2- (methoxy)ethyl]glycinamide 471

1-acetyl-N-3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl) piperidine-4-carboxamide 472

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2-(2- methylpyrrolidin-1-yl) acetamide 473

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)furan- 3-carboxamide 474

N-2-,N-2-dimethyl-N-(3- {[(3-{[3-(methoxy)phenyl] amino}quinoxalin-2-yl) amino]sulfonyl}phenyl) glycinamide 475

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-6- chloropyridine-3- carboxamide 476

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2- chlorobenzamide 477

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2- pyridin-2-ylacetamide 478

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2-[3- (dimethylamino) azetidin-1-yl]acetamide 479

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2- pyridin-3-ylacetamide 480

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2-(2- chlorophenyl)acetamide 481

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-[3- (dimethylamino)propyl]-N- 2-methylglycinamide 482

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- ethyl-N-2-(2-hydroxyethyl) glycinamide 483

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2-[2- (phenylmethyl) pyrrolidin-1-yl]acetamide 484

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl) propanamide 485

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)furan- 2-carboxamide 486

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2- chloropyridine-4- carboxamide 487

N-2-acetyl-N-(3-{[(3-{[3,5- bis(methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)glycinamide 488

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)butanamide 489

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-4- chlorobenzamide 490

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-4- methylbenzamide 491

1,1-dimethylethyl{2-[(3- {[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin- 2-yl)amino]sulfonyl} phenyl)amino]-2-oxoethyl} carbamate 492

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-1,3- benzodioxole-5-carboxamide 493

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-({[2- (methoxy)phenyl]methyl} oxy)glycinamide 494

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl) pyridine-4-carboxamide 495

N-(3-{[(3-{[4-fluoro-3- (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2-, N-2-dimethylglycinamide 496

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2-[4-(3,4- dichlorophenyl)piperazin- 1-yl]acetamide 497

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-3- pyridin-3-ylpropanamide 498

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl) tetrahydrofuran-3- carboxamide 499

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-N-2- [(2-methylphenyl) methyl]glycinamide 500

N-(3-{[(3-{[3,5- bis(methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2- methylbutanamide 501

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2-(3- fluorophenyl)acetamide 502

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-(1-methyl-1-phenylethyl) glycinamide 503

N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino] sulfonyl}phenyl)-2- methylcyclopropanecarboxamide 504

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- methyl-4-(methoxy)benzamide 505

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- methylpyridine-3-carboxamide 506

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-4- (methoxy)benzamide 507

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- (4-ethylpiperazin-1-yl)acetamide 508

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl) thiophene-2-carboxamide 509

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3- fluoro-2-methylbenzamide 510

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- bromothiophene-3-carboxamide 511

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-4- fluorobenzamide 512

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2-(3- methylpiperidin-1-yl)acetamide 513

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- methylpropanamide 514

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl) pentanamide 515

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- (ethyloxy)acetamide 516

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-(2-fluorophenyl)glycinamide 517

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3- (dimethylamino)benzamide 518

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2-(4- methylpiperidin-1-yl)acetamide 519

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-(2-propylphenyl)glycinamide 520

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl) benzamide 521

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl) pyrazine-2-carboxamide 522

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3- fluoro-4-(methoxy)benzamide 523

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2,2- dimethylbutanamide 524

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- [(4-fluorophenyl)oxy]acetamide 525

1-acetyl-N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino]sulfonyl} phenyl)azetidine-3-carboxamide 526

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-N-2- (4-methylphenyl)glycinamide 527

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-phenylglycinamide 528

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)- 2-(4-prop-2-en-1-ylpiperazin- 1-yl)acetamide 529

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- methylbenzamide 530

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3- (methoxy)propanamide 531

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3- methylfuran-2-carboxamide 532

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)- 2,2-dimethylpropanamide 533

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N-2- [(phenylmethyl)oxy]glycinamide 534

N-(3-[({3-[(2-chloro-5- hydroxyphenyl)amino] quinoxalin-2-yl}amino)sulfonyl] phenyl}-N-2-,N-2- dimethylglycinamide 535

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-N-2- (3-chlorophenyl)glycinamide 536

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl) cyclobutanecarboxamide 537

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2-[3- (methoxy)phenyl]acetamide 538

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-1- methylcyclopropanecarboxamide 539

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3- fluorobenzamide 540

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-4- (dimethylamino)benzamide 541

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3,4- dichlorobenzamide 542

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N-2- {[2-(methylthio)phenyl]methyl} glycinamide 543

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- (2-fluorophenyl)acetamide 544

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-ethyl-N-2-(1-methylethyl) glycinamide 545

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-1,3- thiazole-4-carboxamide 546

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-methyl-N-2-(phenylmethyl) glycinamide 547

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-(2-thienylmethyl)glycinamide 548

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N-2- (pyridin-2-ylmethyl)glycinamide 549

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3- (methoxy)benzamide 550

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-[(3-chloro-4-methylphenyl) methyl]glycinamide 551

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- methylpentanamide 552

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- (4-chlorophenyl)acetamide 553

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3- fluoro-4-methylbenzamide 554

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-2-[(2- methylphenyl)oxy]acetamide 555

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- cyclohexylacetamide 556

(1R,2R)-N-(3-{[(3-{[3,5-bis (methoxy)phenyl]amino} quinoxalin-2-yl)amino]sulfonyl} phenyl)-2- phenylcyclopropanecarboxamide 557

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3- chlorobenzamide 558

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2-[2- (methoxy)phenyl]acetamide 559

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3-[3- (methoxy)phenyl]propanamide 560

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-(2-fluoro-4-methylphenyl) glycinamide 561

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-[(3-fluorophenyl)methyl] glycinamide 562

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- [4-(methoxy)phenyl]acetamide 563

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- phenylacetamide 564

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2,4- dichlorobenzamide 565

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3- oxocyclohexanecarboxamide 566

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N-2- (3-fluorophenyl)glycinamide 567

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- (3-chlorophenyl)acetamide 568

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N-2- (2-phenylpropyl)glycinamide 569

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N-2- [(2,4-dimethylphenyl)methyl] glycinamide 570

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2-(2- methylpiperidin-1-yl)acetamide 571

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-[2-(methoxy)phenyl] glycinamide 572

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- (3,4-dihydroisoquinolin- 2-(1H)-yl)acetamide 573

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl) pent-4-enamide 574

N-3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-(2-methylphenyl)glycinamide 575

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)- 2-(4-oxopiperidin-1-yl)acetamide 576

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- fluorobenzamide 577

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- y])amino]sulfonyl}phenyl)-N- 2-(1-phenylethyl)glycinamide 578

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- fluoro-6-(methoxy)benzamide 579

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N-2- [2-(1-methylethyl)phenyl] glycinamide 580

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-3-[2- (methoxy)phenyl]propanamide 581

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)- 4-methylpentanamide 582

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2-(2- phenylmorpholin-4-yl)acetamide 583

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-3-[4- (methoxy)phenyl]propanamide 584

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-cyclopentyl-N-2-prop-2-en- 1-ylglycinamide 585

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-methyl-N-2-[2-(methoxy) ethyl]glycinamide 586

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-4- cyclopropyl-4-oxobutanamide 587

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-[3-(1,1-dimethylethyl) phenyl]glycinamide 588

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-(cyclopropylmethyl)-N- 2-propylglycinamide 589

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- (2-oxocyclopentyl)acetamide 590

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-(4-chlorophenyl)glycinamide 591

2-(1,4′-bipiperidin-1′-yl)-N-(3- {[(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)amino] sulfonyl}phenyl)acetamide 592

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)- 2-(4-cyclopentylpiperazin- 1-yl)acetamide 593

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)- 2-(2-methylphenyl)acetamide 594

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-[(5-fluoro-2-methylphenyl) methyl]glycinamide 595

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3,3- dimethylbutanamide 596

N-(3-{[(3-{[3,5-bis(methyloxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N²- (2-chlorophenyl)glycinamide 597

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-5- fluoro-2-methylbenzamide 598

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)- 4-fluoro-3-methylbenzamide 599

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)- 2,3-dichlorobenzamide 600

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- (phenyloxy)acetamide 601

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-N-2- (2,3-dimethylphenyl)glycinamide 602

3-amino-N-(3-{[3,5-bis(methoxy) phenyl]amino}pyrido[2,3-b] pyrazin-2-yl)benzenesulfonamide 603

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)- 2-fluoro-5-methylbenzamide 604

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N-2- {[(4-methylphenyl)methyl]oxy} glycinamide 605

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- [4-(1-methylethyl)piperazin- 1-yl]acetamide 606

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)- 2-(4-fluorophenyl)acetamide 607

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3- methylbutanamide 608

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-4- methyl-2-(methoxy)benzamide 609

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-2-(4- propylpiperidin-1-yl)acetamide 610

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- [(3-methylphenyl)oxy]acetamide 611

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl) tetrahydrofuran-2-carboxamide 612

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- [3-(hydroxymethyl)piperidin- 1-yl]acetamide 613

1,1-dimethylethyl2-{[(3-{[(3- {[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)amino] sulfonyl}phenyl)amino]carbonyl} piperidine-1-carboxylate 614

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-methyl-N-2-(pyridin-3- ylmethyl)glycinamide 615

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-N- 2-ethyl-N-2-phenylglycinamide 616

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-2-{[2- (methoxy)ethyl]oxy}acetamide 617

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)- 3-cyclopentylpropanamide 618

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)- 2,5-dichlorobenzamide 619

2-(4-acetylpiperazin-1-yl)-N-(3- {[(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)amino] sulfonyl}phenyl)acetamide 620

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-5- fluoro-2-(methoxy)benzamide 621

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-N-2- cyclohexyl-N-2-ethylglycinamide 622

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-5- methylisoxazole-3-carboxamide 623

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3- methylpyridine-2-carboxamide 624

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}phenyl)-2- (methoxy)pyridine-3- carboxamide 625

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-3,5- dichlorobenzamide 626

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- (1,3-thiazolidin-3-yl)acetamide 627

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2-(4- formylpiperazin-1-yl)acetamide 628

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- (2-pyridin-4-ylpiperidin-1- yl)acetamide 629

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)- 2-(methoxy)benzamide 630

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)- N-2-methyl-N-2-(2- methylpropyl)glycinamide 631

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- (4-formyl-1,4-diazepan-1- yl)acetamide 632

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-1- phenylcyclopropanecarboxamide 633

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- (2,6-dimethylmorpholin-4- yl)acetamide 634

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2- (2-phenylpyrrolidin-1-yl) acetamide 635

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[2- (dimethylamino)-1-methylethyl] benzamide 636

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[2- (dimethylamino)ethyl]benzamide 637

5-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[2- (dimethylamino)ethyl]-2- fluorobenzamide 638

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-pyrrolidin- 3-ylbenzamide 639

3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[2- (dimethylamino)ethyl] benzamide 640

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(2- pyrrolidin-1-ylethyl)benzamide 641

N-(2-aminoethyl)-3-{[(3-{[2- chloro-5-(methoxy)phenyl] amino}quinoxalin-2-yl) amino]sulfonyl}benzamide 642

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[2- (dimethylamino)ethyl]-N- methylbenzamide 643

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N- (piperidin-2-ylmethyl) benzamide 644

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(1- methylazetidin-3-yl)benzamide 645

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(2- piperidin-1-ylethyl)benzamide 646

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[2- (diethylamino)ethyl]benzamide 647

3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[2- (dimethylamino)ethyl]-N- methylbenzamide 648

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(1- methylpiperidin-3-yl)benzamide 649

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-piperidin- 3-ylbenzamide 650

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[(1- methylpiperidin-2-yl)methyl] benzamide 651

N-{2-[bis(2-hydroxyethyl) amino]ethyl}-3-{[(3-{[2- chloro-5-(methoxy)phenyl] amino}quinoxalin-2- yl)amino]sulfonyl}benzamide 652

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(1- ethylpiperidin-3-yl)benzamide 653

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}benzamide 654

3-[(3-aminopyrrolidin-1-yl) carbonyl]-N-(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl) benzenesulfonamide 655

5-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[2- (dimethylamino)ethyl]-2- (methoxy)benzamide 656

N-(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2-yl)- 3-{[3-(methylamino)pyrrolidin-1- yl]carbonyl}benzenesulfonamide 657

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}benzoicacid 658

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(2- morpholin-4-ylethyl)benzamide 659

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[(1- ethylpyrrolidin-2-yl)methyl] benzamide 660

3-[(4-amino-3-oxopyrazolidin- 1-yl)carbonyl]-N-(3-{[2-chloro- 5-(methoxy)phenyl]amino} quinoxalin-2-yl) benzenesulfonamide 661

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}-N- methylbenzamide 662

3-[(3-aminoazetidin-1-yl) carbonyl]-N-(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl) benzenesulfonamide 663

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(pyridin- 3-ylmethyl)benzamide 664

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(pyridin- 2-ylmethyl)benzamide 665

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(2- hydroxyethyl)benzamide 666

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(3- oxopyrazolidin-4-yl)benzamide 667

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[2-(1H- imidazol-4-yl)ethyl]benzamide 668

N-(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)-3-{[3-(dimethylamino) pyrrolidin-1-yl]carbonyl} benzenesulfonamide 669

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N- (pyridin-4-ylmethyl)benzamide 670

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-methyl- N-(1-methylpyrrolidin-3-yl) benzamide 671

N-(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2-yl)- 3-{[3-(diethylamino)pyrrolidin- 1-yl]carbonyl} benzenesulfonamide 672

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-1H- pyrrol-1-ylbenzamide 673

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(3- pyrrolidin-1-ylpropyl)benzamide 674

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}-N-(2- cyanoethyl)-N-methylbenzamide 675

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[2- (methoxy)ethyl]benzamide 676

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(2- cyanoethyl)-N-ethylbenzamide 677

3-[(3-aminopiperidin-1-yl) carbonyl]-N-(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl) benzenesulfonamide 678

3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfony}benzoicacid 679

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}-N-[3- (dimethylamino)propyl] benzamide 680

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N- morpholin-4-ylbenzamide 681

N-(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)-3-[(2,2-dimethylhydrazino) carbonyl]benzenesulfonamide 682

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[3-(1H- imidazol-1-yl)propyl]benzamide 683

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[3- (diethylamino)propyl]benzamide 684

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(2- cyanoethyl)benzamide 685

methylN-[(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino]sulfonyl} phenyl)carbonyl]-beta-alaninate 686

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[2- (methylthio)ethyl]benzamide 687

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[2- (ethylthio)ethyl]benzamide 688

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[2- (dimethylamino)ethyl]- N-ethylbenzamide 689

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N[3-(2- oxopyrrolidin-1-yl)propyl] benzamide 690

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(2- pyridin-4-ylethyl)benzamide 691

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[3- (ethyloxy)propyl]benzamide 692

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(3- morpholin-4-ylpropyl) benzamide 693

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[3- (methoxy)propyl]benzamide 694

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[3- (dimethylamino)propyl]-N- methylbenzamide 695

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[3- (propyloxy)propyl]benzamide 696

ethylN-[(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino]sulfonyl} phenyl)carbonyl]-beta-alaninate 697

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-{3-[(1- methylethyl)oxy]propyl} benzamide 698

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(1,1- dimethyl-2-piperidin-1- ylethyl)benzamide 699

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-methyl- N-propylbenzamide 700

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N- piperidin-1-ylbenzamide 701

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[1- methyl-2-(methoxy)ethyl] benzamide 702

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2-yl) amino]sulfonyl}-N-(1,1- dimethyl-2-morpholin-4-ylethyl) benzamide 703

N-(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)-3-({2-[(dimethylamino) methyl]piperidin-1-yl}carbonyl) benzenesulfonamide 704

N-[3-(butyloxy)propyl]-3-{[(3- {[2-chloro-5-(methoxy)phenyl] amino}quinoxalin-2-yl) amino]sulfonyl}benzamide 705

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-[4- (diethylamino)-1-methylbutyl] benzamide 706

3-{[(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}-N-(1,1-dimethyl- 2-oxo-2-piperidin-1-ylethyl) benzamide 707

N-(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)-3-[(4-methylpiperazin-1- yl)carbonyl]benzenesulfonamide 708

N-(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)-3-{[2-(piperidin-1-ylmethyl) piperidin-1-yl]carbonyl} benzenesulfonamide 709

N-(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)-6-oxo-1,6-dihydropyridine- 3-sulfonamide 710

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)- 6-oxo-1,6-dihydropyridine-3- sulfonamide 711

3-amino-N-(3-{[6-(methoxy) quinolin-8-yl]amino}quinoxalin- 2-yl)benzenesulfonamide 712

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl) thiophene-2-sulfonamide 713

N-(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)-3-cyanobenzenesulfonamide 714

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-3- (methylamino) benzenesulfonamide 715

N-(2-{[3,5-bis(methoxy)phenyl] amino}pyrido[2,3-b]pyrazin-3- yl)-3-nitrobenzenesulfonamide 716

N-(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)-3-(1-{[2-(dimethylamino) ethyl]amino}ethyl) benzenesulfonamide 717

3-amino-N-(3-{[3-(methoxy)-5- nitrophenyl]amino}quinoxalin- 2-yl)benzenesulfonamide 718

3-acetyl-N-(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl) benzenesulfonamide 719

3-amino-N-(3-{[3-fluoro-5- (methoxy)phenyl]amino} quinoxalin-2-yl) benzenesulfonamide 720

N-(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2-yl)- N′-[2-(dimethylamino)ethyl] benzene-1,3-disulfonamide 721

N-(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2-yl)- N′-[3-(dimethylamino)propyl] benzene-1,3-disulfonamide 722

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-6- chloropyridine-3-sulfonamide 723

N-(3-{[2-chloro-5-(methoxy) phenyl]amino}quinoxalin-2- yl)-3-{5-[(dimethylamino) methyl]-1,3,4-oxadiazol-2- yl}benzenesulfonamide 724

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-6-{[2- (dimethylamino)ethyl]amino} pyridine-3-sulfonamide 725

3-amino-N-(3-{[3-amino-5- (methoxy)phenyl]amino} quinoxalin-2-yl) benzenesulfonamide 726

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-3- (dimethylamino) benzenesulfonamide 727

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-6- {[2-(dimethylamino)ethyl] oxy}pyridine-3-sulfonamide 728

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-6- (dimethylamino)pyridine-3- sulfonamide 729

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)- 4-cyanobenzenesulfonamide 730

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)- 4-fluorobenzenesulfonamide 731

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-4-fluoro- 2-methylbenzenesulfonamide 732

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)- 2-methylbenzenesulfonamide 733

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)- 3-cyanobenzenesulfonamide 734

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-3,5- difluorobenzenesulfonamide 735

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)- 2-chlorobenzenesulfonamide 736

N-(4-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl) acetamide 737

N-(3-{[6-(methoxy)quinolin-8- yl]amino}quinoxalin-2-yl)-3- nitrobenzenesulfonamide 738

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-3-(2H- tetrazol-5-yl)benzenesulfonamide 739

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl) naphthalene-1-sulfonamide 740

N-{[(3-{[(3-{[2-chloro-5- (methoxy)phenyl]amino} quinoxalin-2-yl)amino]sulfonyl}- 4-methylphenyl)amino] (dimethylamino)methylidene}- N-methylmethanaminium 741

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)- 3-fluorobenzenesulfonamide 742

N-(3-{[2-bromo-5-(methoxy) phenyl]amino}quinoxalin-2-yl)- 3-nitrobenzensulfonamide 743

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-4- [(difluoromethyl)oxy] benzenesulfonamide 744

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-2- (trifluoromethyl) benzenesulfonamide 745

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-3-chloro- 4-fluorobenzensulfonamide 746

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-4- (trifluoromethyl) benzenesulfonamide 747

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-3- (methylsulfonyl) benzenesulfonamide 748

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-2,5- dichlorthiophene-3-sulfonamide 749

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-3,5- dichlorobenzenesulfonamide 750

N-(3-{[2-methyl-5-(methoxy) phenyl]amino}quinoxalin-2-yl)- 3-nitrobenzenesulfonamide 751

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-4- [(trifluoromethyl)oxy] benzensulfonamide 752

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-2-[4- (dimethylamino)piperidin-1-yl] acetamide 753

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-5- chloro-2-(methoxy) benzenesulfonamide 754

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-3- (trifluoromethyl) benzenesulfonamide 755

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-2,5-bis (methoxy)benzenesulfonamide 756

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-3,5- dimethylisoxazole-4-sulfonamide 757

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-5-bromo- 2-(methoxy)benzenesulfonamide 758

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-4- fluoro-3-(trifluoromethyl) benzenesulfonamide 759

N-(3-{[3-fluoro-5-(methoxy) phenyl]amino}quinoxalin-2-yl)- 3-nitrobenzenesulfonamide 760

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-3-fluoro- 4-methylbenzenesulfonamide 761

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-3-chloro- 4-methylbenzenesulfonamide 762

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-2,5- dimethylthiophene-3-sulfonamide 763

N-(3-{[3-(methoxy)phenyl] amino}quinoxalin-2-yl)-3- nitrobenzenesulfonamide 764

N-{3-[(2-chloro-5- hydroxyphenyl)amino]quinoxalin- 2-yl}-3-nitrobenzenesulfonamide 765

N-(3-{[(3-{[3,5-bis(methoxy) phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)-4- methyl-3-(methoxy)benzamide 766

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-1- phenylmethanesulfonamide 767

N-(3-{[3-(methoxy)-5- nitrophenyl]amino}quinoxalin-2- yl)-3-nitrobenzenesulfonamide 768

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-1-(3- chlorophenyl) methanesulfonamide 769

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-4,5- dichlorothiophene-2-sulfonamide 770

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-5- chloro-1,3-dimethyl-1H- pyrazole-4-sulfonamide 771

N-(3-{[3,5-bis(methoxy)phenyl] amino}quinoxalin-2-yl)-3,5-bis (trifluoromethyl) benzenesulfonamide

Table 2a Representative AKT Inhibitors

The Compounds in Table 2a can be prepared as pharmaceutically acceptable salts, solvates, hydrates, and/or isomers thereof. All such salt, solvate, hydrate, and isomer combinations of the Compounds in Table 2a can be used to practice the invention.

Cmpd No. Name 1 3-(azetidin-3-ylidenemethyl)-4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H- pyrazolo[3,4-d]pyrimidine 2 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-(3-fluoropyridin-4-yl)-1H-pyrazolo[3,4- d]pyrimidine 3 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-(3-chloropyridin-4-yl)-1H-pyrazolo[3,4- d]pyrimidine 4 2-({5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- methylphenyl}oxy)-N,N-dimethylethanamine 5 2-({5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- methylphenyl}oxy)-N,N-diethylethanamine 6 4-(4-{5-chloro-2-methyl-3-[(2-pyrrolidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)-3-ethyl- 1H-pyrazolo[3,4-d]pyrimidine 7 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-piperazin-1-yl-1H-pyrazolo[3,4- d]pyrimidine 8 N-(3-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-3- yl}prop-2-yn-1-yl)acetamide 9 N,N-diethyl-2-({3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1- yl]phenyl}oxy)ethanamine 10 3-{3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-chloro-2- methylphenyl}-N,N-diethylpropan-1-amine 11 3-bromo-4-{4-[5-chloro-2-methyl-3-(3-pyrrolidin-1-ylpropyl)phenyl]piperazin-1-yl}-1H- pyrazolo[3,4-d]pyrimidine 12 3-bromo-4-(4-{5-chloro-2-methyl-3-[(2-pyrrolidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)- 1H-pyrazolo[3,4-d]pyrimidine 13 2-({3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-chloro-2- methylphenyl}oxy)-N,N-diethylethanamine 14 4-[4-(5-chloro-2-methyl-3-{[2-(1-methylpiperidin-4-yl)ethyl]oxy}phenyl)piperazin-1-yl]- 3-ethyl-1H-pyrazolo[3,4-d]pyrimidine 15 5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-N-(2- pyrrolidin-1-ylethyl)aniline 16 4-(4-{5-chloro-2-methyl-3-[(2-morpholin-4-ylethyl)oxy]phenyl}piperazin-1-yl)-3-ethyl- 1H-pyrazolo[3,4-d]pyrimidine 17 4-(4-{5-chloro-2-methyl-3-[(2-piperidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)-3-ethyl-1H- pyrazolo[3,4-d]pyrimidine 18 3-bromo-4-{4-[5-chloro-2-methyl-3-(3-morpholin-4-ylpropyl)phenyl]piperazin-1-yl}-1H- pyrazolo[3,4-d]pyrimidine 19 3-bromo-4-(4-{5-chloro-2-methyl-3-[3-(4-methylpiperazin-1-yl)propyl]phenyl}piperazin- 1-yl)-1H-pyrazolo[3,4-d]pyrimidine 20 3-bromo-4-(4-{5-chloro-2-methyl-3-[(2-piperidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)- 1H-pyrazolo[3,4-d]pyrimidine 21 3-bromo-4-(4-{5-chloro-2-methyl-3-[(2-morpholin-4-ylethyl)oxy]phenyl}piperazin-1-yl)- 1H-pyrazolo[3,4-d]pyrimidine 22 4-{4-[5-chloro-2-methyl-3-(3-morpholin-4-ylpropyl)phenyl]piperazin-1-yl}-3-ethyl-1H- pyrazolo[3,4-d]pyrimidine 23 N′-{5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- methylphenyl}-N,N-diethylethane-1,2-diamine 24 4-{4-[5-chloro-2-methyl-3-(3-piperidin-1-ylpropyl)phenyl]piperazin-1-yl}-3-ethyl-1H- pyrazolo[3,4-d]pyrimidine 25 4-[4-(5-chloro-3-{[2-(4-ethylpiperazin-1-yl)ethyl]oxy}-2-methylphenyl)piperazin-1-yl]-3- ethyl-1H-pyrazolo[3,4-d]pyrimidine 26 4-(4-{5-chloro-2-methyl-3-[(3-morpholin-4-ylpropyl)oxy]phenyl}piperazin-1-yl)-3-ethyl- 1H-pyrazolo[3,4-d]pyrimidine 27 3-bromo-4-{4-[5-chloro-2-methyl-3-(3-piperidin-1-ylpropyl)phenyl]piperazin-1-yl}-1H- pyrazolo[3,4-d]pyrimidine 28 N′-{3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-chloro-2- methylphenyl}-N,N-diethylethane-1,2-diamine 29 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-chloro-2-methyl-N-(2- pyrrolidin-1-ylethyl)aniline 30 4-[4-(5-chloro-2-methyl-3-{[2-(4-methylpiperazin-1-yl)ethyl]oxy}phenyl)piperazin-1-yl]- 3-ethyl-1H-pyrazolo[3,4-d]pyrimidine 31 4-[4-(5-chloro-2-methyl-3-{[(1-methylpiperidin-4-yl)methyl]oxy}phenyl)piperazin-1-yl]-3- ethyl-1H-pyrazolo[3,4-d]pyrimidine 32 N,N-diethyl-2-({3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- methylphenyl}oxy)ethanamine 33 2-[(5-chloro-3-{4-[1-(1,1-dimethylethyl)-3-(trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidin- 4-yl]piperazin-1-yl}-2-methylphenyl)oxy]-N,N-diethylethanamine 34 2-[(5-chloro-2-methyl-3-{4-[3-(trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidin-4- yl]piperazin-1-yl}phenyl)oxy]-N,N-diethylethanamine 35 4-(4-{5-chloro-2-methyl-3-[(3-pyrrolidin-1-ylpropyl)oxy]phenyl}piperazin-1-yl)-3-ethyl- 1H-pyrazolo[3,4-d]pyrimidine 36 4-[4-(5-chloro-2-methyl-3-{[3-(4-methylpiperazin-1-yl)propyl]oxy}phenyl)piperazin-1-yl]- 3-ethyl-1H-pyrazolo[3,4-d]pyrimidine 37 3-bromo-4-(4-{5-chloro-2-methyl-3-[(3-piperidin-1-ylpropyl)oxy]phenyl}piperazin-1-yl)- 1H-pyrazolo[3,4-d]pyrimidine 38 3-bromo-4-(4-{5-chloro-2-methyl-3-[(3-morpholin-4-ylpropyl)oxy]phenyl}piperazin-1-yl)- 1H-pyrazolo[3,4-d]pyrimidine 39 4-(4-{5-chloro-2-methyl-3-[(2-pyrrolidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)-3- (trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidine 40 4-(4-{5-chloro-2-methyl-3-[(3-morpholin-4-ylpropyl)oxy]phenyl}piperazin-1-yl)-3- (trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidine 41 4-(4-{5-chloro-2-methyl-3-[(2-morpholin-4-ylethyl)oxy]phenyl}piperazin-1-yl)-3- (trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidine 42 4-(4-{5-chloro-2-methyl-3-[(3-piperidin-1-ylpropyl)oxy]phenyl}piperazin-1-yl)-3-ethyl- 1H-pyrazolo[3,4-d]pyrimidine 43 4-[4-(5-chloro-3-{[3-(4-ethylpiperazin-1-yl)propyl]oxy}-2-methylphenyl)piperazin-1-yl]-3- ethyl-1H-pyrazolo[3,4-d]pyrimidine 44 5-chloro-2-methyl-3-[4-(1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N-(2- pyrrolidin-1-ylethyl)aniline 45 5-chloro-2-methyl-3-[4-(3-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N-(2- pyrrolidin-1-ylethyl)aniline 46 N′-(5-chloro-2-methyl-3-{4-[3-(trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidin-4- yl]piperazin-1-yl}phenyl)-N,N-dimethylethane-1,2-diamine 47 3-({5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- methylphenyl}oxy)-N,N-diethylpropan-1-amine 48 N′-(5-chloro-2-methyl-3-{4-[3-(trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidin-4- yl]piperazin-1-yl}phenyl)-N,N-diethylethane-1,2-diamine 49 5-chloro-2-methyl-N-(2-pyrrolidin-1-ylethyl)-3-{4-[3-(trifluoromethyl)-1H-pyrazolo[3,4- d]pyrimidin-4-yl]piperazin-1-yl}aniline 50 3-bromo-4-(4-{4-methyl-3-[(2-pyrrolidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)-1H- pyrazolo[3,4-d]pyrimidine 51 4-(4-{4-methyl-3-[(2-pyrrolidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)-1H-pyrazolo[3,4- d]pyrimidine 52 3-methyl-4-(4-{4-methyl-3-[(2-pyrrolidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)-1H- pyrazolo[3,4-d]pyrimidine 53 4-(4-{5-chloro-2-methyl-3-[(2-pyrrolidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)-1H- pyrazolo[3,4-d]pyrimidine 54 4-(4-{5-chloro-2-methyl-3-[(2-pyrrolidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)-3-methyl- 1H-pyrazolo[3,4-d]pyrimidine 55 4-(4-{5-chloro-2-methyl-3-[(2-piperidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)-3- (trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidine 56 3-[(5-chloro-2-methyl-3-{4-[3-(trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidin-4- yl]piperazin-1-yl}phenyl)oxy]-N,N-diethylpropan-1-amine 57 5-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-N-(2- pyrrolidin-1-ylethyl)aniline 58 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-fluoro-2-methyl-N-(2- pyrrolidin-1-ylethyl)aniline 59 4-{4-[5-chloro-2-methyl-3-(3-pyrrolidin-1-ylpropyl)phenyl]piperazin-1-yl}-1H- pyrazolo[3,4-d]pyrimidine 60 3-bromo-4-{4-[5-fluoro-2-methyl-3-(3-pyrrolidin-1-ylpropyl)phenyl]piperazin-1-yl}-1H- pyrazolo[3,4-d]pyrimidine 61 4-{4-[5-chloro-2-methyl-3-(3-pyrrolidin-1-ylpropyl)phenyl]piperazin-1-yl}-3- (trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidine 62 4-(4-{5-chloro-2-methyl-3-[3-(4-methylpiperazin-1-yl)propyl]phenyl}piperazin-1-yl)-3- ethyl-1H-pyrazolo[3,4-d]pyrimidine 63 3-bromo-4-(4-pyridin-2-ylpiperazin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine 64 3-bromo-4-[4-(2,4-dimethylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 65 3-bromo-4-{4-[3-(methyloxy)phenyl]piperazin-1-yl}-1H-pyrazolo[3,4-d]pyrimidine 66 3-bromo-4-{4-[2-(methyloxy)phenyl]piperazin-1-yl}-1H-pyrazolo[3,4-d]pyrimidine 67 3-bromo-4-{4-[4-methyl-3-(3-pyrrolidin-1-ylpropyl)phenyl]piperazin-1-yl}-1H- pyrazolo[3,4-d]pyrimidine 68 4-(4-{5-chloro-2-methyl-3-[(3-pyrrolidin-1-ylpropyl)oxy]phenyl}piperazin-1-yl)-3- (trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidine 69 4-(4-{5-chloro-2-methyl-3-[(3-piperidin-1-ylpropyl)oxy]phenyl}piperazin-1-yl)-3- (trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidine 70 4-[4-(5-chloro-2-methyl-3-{[3-(4-methylpiperazin-1-yl)propyl]oxy}phenyl)piperazin-1-yl]- 3-(trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidine 71 4-[4-(5-chloro-3-{[3-(4-ethylpiperazin-1-yl)propyl]oxy}-2-methylphenyl)piperazin-1-yl]-3- (trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidine 72 3-bromo-4-[4-(5-chloro-2-methyl-3-{[2-(4-methylpiperazin-1- yl)ethyl]oxy}phenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 73 4-[4-(5-chloro-2-methyl-3-{[2-(4-methylpiperazin-1-yl)ethyl]oxy}phenyl)piperazin-1-yl]- 3-(trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidine 74 3-bromo-4-[4-(5-chloro-3-{[2-(4-ethylpiperazin-1-yl)ethyl]oxy}-2- methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 75 3-bromo-4-[4-(3,4-dichlorophenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 76 3-bromo-4-[4-(3,4-difluorophenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 77 3-bromo-4-[4-(2,4-dichlorophenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 78 3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-fluoro-2-methyl-N-(2- pyrrolidin-1-ylethyl)aniline 79 5-fluoro-2-methyl-N-(2-pyrrolidin-1-ylethyl)-3-{4-[3-(trifluoromethyl)-1H-pyrazolo[3,4- d]pyrimidin-4-yl]piperazin-1-yl}aniline 80 4-{4-[3,5-bis(methyloxy)phenyl]piperazin-1-yl}-3-bromo-1H-pyrazolo[3,4-d]pyrimidine 81 4-[4-(5-chloro-3-{[2-(4-ethylpiperazin-1-yl)ethyl]oxy}-2-methylphenyl)piperazin-1-yl]-3- (trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidine 82 N-{5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- methylphenyl}-N,N′,N′-trimethylethane-1,2-diamine 83 3-({3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-chloro-2- methylphenyl}oxy)-N,N-diethylpropan-1-amine 84 3-bromo-4-(4-{5-chloro-2-methyl-3-[(3-pyrrolidin-1-ylpropyl)oxy]phenyl}piperazin-1-yl)- 1H-pyrazolo[3,4-d]pyrimidine 85 3-bromo-4-[4-(5-chloro-2-methyl-3-{[3-(4-methylpiperazin-1- yl)propyl]oxy}phenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 86 3-bromo-4-[4-(5-chloro-3-{[3-(4-ethylpiperazin-1-yl)propyl]oxy}-2- methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 87 3-(5-chloro-2-methyl-3-{4-[3-(trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidin-4- yl]piperazin-1-yl}phenyl)-N,N-diethylpropan-1-amine 88 3-bromo-4-[4-(5-chloro-2-methyl-3-{[(1-methylpiperidin-4- yl)methyl]oxy}phenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 89 3-bromo-4-[4-(5-chloro-2-methyl-3-{[2-(1-methylpiperidin-4- yl)ethyl]oxy}phenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 90 4-[4-(5-chloro-2-methyl-3-{[(1-methylpiperidin-4-yl)methyl]oxy}phenyl)piperazin-1-yl]-3- (trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidine 91 4-[4-(5-chloro-2-methyl-3-{[2-(1-methylpiperidin-4-yl)ethyl]oxy}phenyl)piperazin-1-yl]- 3-(trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidine 92 4-(4-{5-chloro-2-methyl-3-[3-(4-methylpiperazin-1-yl)propyl]phenyl}piperazin-1-yl)-3- (trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidine 93 3-bromo-4-[4-(3-chloro-4-fluorophenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 94 1-{4-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]phenyl}ethanone 95 3-bromo-4-[4-(2,5-dichlorophenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 96 3-bromo-4-[4-(3,4-dimethylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 97 3-bromo-4-[4-(4-nitrophenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 98 3-ethyl-4-(4-phenylpiperazin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine 99 3-ethyl-4-{4-[3-(methyloxy)phenyl]piperazin-1-yl}-1H-pyrazolo[3,4-d]pyrimidine 100 4-{4-[5-chloro-2-methyl-3-(3-piperidin-1-ylpropyl)phenyl]piperazin-1-yl}-3- (trifluoromethyl)-1H-pyrazolo[3,4-d]pyrimidine 101 4-[4-(3,6-dimethylpyrazin-2-yl)piperazin-1-yl]-3-ethyl-1H-pyrazolo[3,4-d]pyrimidine 102 1-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]isoquinoline 103 3-bromo-4-[4-(2,6-dimethylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 104 3-bromo-4-{4-[4-(ethyloxy)phenyl]piperazin-1-yl}-1H-pyrazolo[3,4-d]pyrimidine 105 3-bromo-4-[4-(2-ethylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 106 4-{4-[2,4-bis(methyloxy)phenyl]piperazin-1-yl}-3-bromo-1H-pyrazolo[3,4-d]pyrimidine 107 3-bromo-4-(4-pyrazin-2-ylpiperazin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine 108 3-bromo-4-(4-pyrimidin-2-ylpiperazin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine 109 4-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- (trifluoromethyl)quinoline 110 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]pyrazine-2-carbonitrile 111 4-[4-(4,6-dimethylpyrimidin-2-yl)piperazin-1-yl]-3-ethyl-1H-pyrazolo[3,4-d]pyrimidine 112 ethyl 4-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- (trifluoromethyl)pyrimidine-5-carboxylate 113 4-{4-[3-chloro-5-(methyloxy)phenyl]piperazin-1-yl}-3-ethyl-1H-pyrazolo[3,4- d]pyrimidine 114 4-[4-(3-bromo-2-chloro-5-fluorophenyl)piperazin-1-yl]-3-ethyl-1H-pyrazolo[3,4- d]pyrimidine 115 2-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]pyridine-3-carboxamide 116 3-ethyl-4-{4-[4-(trifluoromethyl)pyridin-2-yl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 117 3-bromo-4-{4-[4-(trifluoromethyl)pyridin-2-yl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 118 3-bromo-4-{4-[4-(trifluoromethyl)pyrimidin-2-yl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 119 2-({3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]pyrazin-2-yl}oxy)- N,N-dimethylethanamine 120 4-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methylquinoline 121 3-bromo-4-[4-(2-nitrophenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 122 2-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]benzonitrile 123 4-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]benzonitrile 124 3-bromo-4-{4-[4-(trifluoromethyl)phenyl]piperazin-1-yl}-1H-pyrazolo[3,4-d]pyrimidine 125 3-bromo-4-(4-{4-[(phenylmethyl)oxy]phenyl}piperazin-1-yl)-1H-pyrazolo[3,4- d]pyrimidine 126 4-{4-[5-chloro-2-methyl-3-(methyloxy)phenyl]piperazin-1-yl}-3-ethyl-1H-pyrazolo[3,4- d]pyrimidine 127 2-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]pyridine-3-carbonitrile 128 3-bromo-4-[4-(3,5-dichlorophenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 129 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-chloro-5-fluoro-N-(2- pyrrolidin-1-ylethyl)aniline 130 2-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-fluoro-N-(2- pyrrolidin-1-ylethyl)aniline 131 3-bromo-4-[4-(2,5-difluorophenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 132 4-[4-(2,5-difluorophenyl)piperazin-1-yl]-3-ethyl-1H-pyrazolo[3,4-d]pyrimidine 133 3-bromo-4-{4-[3-(methyloxy)pyrazin-2-yl]piperazin-1-yl}-1H-pyrazolo[3,4-d]pyrimidine 134 3-bromo-4-[4-(3-chlorophenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 135 3-bromo-4-{4-[3-(trifluoromethyl)pyridin-2-yl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 136 3-bromo-4-{4-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 137 4-(4-{5-chloro-2-methyl-3-[(2-pyrrolidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)-3-(1- methylethyl)-1H-pyrazolo[3,4-d]pyrimidine 138 5-chloro-2-methyl-3-{4-[3-(1-methylethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl]piperazin-1- yl}-N-(2-pyrrolidin-1-ylethyl)aniline 139 2-({3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]phenyl}oxy)-N- ethylacetamide 140 2-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N,N-diethylpyrimidin-4- amine 141 3-bromo-4-[4-(3-{[(3-methylphenyl)methyl]oxy}phenyl)piperazin-1-yl]-1H-pyrazolo[3,4- d]pyrimidine 142 3-bromo-4-(4-{3-[(2-piperidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)-1H-pyrazolo[3,4- d]pyrimidine 143 3-bromo-4-[4-(4-furan-2-ylpyrimidin-2-yl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 144 6-{2-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]pyrimidin-4-yl}-2H- 1,4-benzoxazin-3(4H)-one 145 3-ethyl-4-{4-[2-methyl-3-(methyloxy)phenyl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 146 N′-{5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- methylphenyl}-N-methyl-N-(1-methylethyl)ethane-1,2-diamine 147 N′-{5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- methylphenyl}-N-ethyl-N-methylethane-1,2-diamine 148 N′-{3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-chloro-2- methylphenyl}-N,N-dimethylethane-1,2-diamine 149 3-({6-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-chloro-5- methylpyrimidin-4-yl}oxy)-N,N-diethylpropan-1-amine 150 3-bromo-4-[4-(2,3-dichlorophenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 151 3-bromo-4-{4-[2-(trifluoromethyl)phenyl]piperazin-1-yl}-1H-pyrazolo[3,4-d]pyrimidine 152 3-bromo-4-(4-phenylpiperazin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine 153 3-bromo-4-[4-(4-fluorophenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 154 3-bromo-4-[4-(4-chlorophenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 155 3-bromo-4-{4-[3-(trifluoromethyl)phenyl]piperazin-1-yl}-1H-pyrazolo[3,4-d]pyrimidine 156 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-6-amine 157 3-bromo-4-[4-(4-bromophenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 158 3-bromo-4-[3-methyl-4-(3-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 159 4-[4-(3-bromo-5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-6- amine 160 4-(4-{5-chloro-2-methyl-3-[(2-pyrrolidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)-3- cyclopropyl-1H-pyrazolo[3,4-d]pyrimidine 161 5-chloro-3-[4-(3-cyclopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl- N-(2-pyrrolidin-1-ylethyl)aniline 162 5-chloro-2-methyl-3-{4-[3-(2-methylpropyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl]piperazin- 1-yl}-N-(2-pyrrolidin-1-ylethyl)aniline 163 4-(4-{5-chloro-2-methyl-3-[(2-pyrrolidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)-3-(2- methylpropyl)-1H-pyrazolo[3,4-d]pyrimidine 164 3-bromo-4-[(3S)-4-(5-chloro-2-methylphenyl)-3-methylpiperazin-1-yl]-1H-pyrazolo[3,4- d]pyrimidine 165 5-bromo-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methylaniline 166 2-({3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]phenyl}oxy)-N- cyclopropylacetamide 167 3-bromo-4-(4-{3-[(2-piperidin-1-ylethyl)oxy]pyrazin-2-yl}piperazin-1-yl)-1H- pyrazolo[3,4-d]pyrimidine 168 4-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-6,7- bis(methyloxy)quinazoline 169 2-({3-chloro-5-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]phenyl}oxy)- N,N-diethylethanamine 170 4-{4-[2-chloro-5-(trifluoromethyl)phenyl]piperazin-1-yl}-3-ethyl-1H-pyrazolo[3,4- d]pyrimidine 171 3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5-[(2- methylpropyl)oxy]-N-(2-pyrrolidin-1-ylethyl)aniline 172 3-({4-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-6-chloro-5- methylpyrimidin-2-yl}oxy)-N,N-diethylpropan-1-amine 173 3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5- [(phenylmethyl)oxy]-N-(2-pyrrolidin-1-ylethyl)aniline 174 3-bromo-4-[(3R)-4-(5-chloro-2-methylphenyl)-3-methylpiperazin-1-yl]-1H-pyrazolo[3,4- d]pyrimidine 175 3-[(2S)-4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-2-methylpiperazin-1-yl]-4-methyl- N-phenylbenzamide 176 3-[(2S)-4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-2-methylpiperazin-1-yl]-4-methyl- N-(phenylmethyl)benzamide 177 methyl 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methylbenzoate 178 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methylbenzoic acid 179 (2E)-3-(4-{4-[5-chloro-2-methyl-3-(3-pyrrolidin-1-ylpropyl)phenyl]piperazin-1-yl}-1H- pyrazolo[3,4-d]pyrimidin-3-yl)prop-2-enoic acid 180 3-(4-{4-[5-chloro-2-methyl-3-(3-pyrrolidin-1-ylpropyl)phenyl]piperazin-1-yl}-1H- pyrazolo[3,4-d]pyrimidin-3-yl)prop-2-yn-1-ol 181 4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-1-(5-chloro-2-methylphenyl)piperazin-2- one 182 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5-[(2- methylpropyl)oxy]-N-(2-pyrrolidin-1-ylethyl)aniline 183 N′-{3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5-[(2- methylpropyl)oxy]phenyl}-N,N-diethylethane-1,2-diamine 184 methyl 3-bromo-5-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4- methylbenzoate 185 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-N- phenylbenzamide 186 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N,4-dimethylbenzamide 187 2-({3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]phenyl}oxy)-N,N- diethylethanamine 188 methyl 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-5-[(2- pyrrolidin-1-ylethyl)amino]benzoate 189 3-bromo-5-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-N- phenylbenzamide 190 3-bromo-5-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-N- phenylbenzamide 191 N′-{3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-chloro-2- methylphenyl}-N-methyl-N-(1-methylethyl)ethane-1,2-diamine 192 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-N-phenyl-5-[(2- pyrrolidin-1-ylethyl)amino]benzamide 193 N′-{3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5-[(2- methylpropyl)oxy]phenyl}-N,N-dimethylethane-1,2-diamine 194 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N,N,4- trimethylbenzamide 195 3-[4-(3-chloro-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-N-(2- methylpropyl)benzamide 196 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N,N,4-trimethyl-5-[(2- pyrrolidin-1-ylethyl)amino]benzamide 197 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-2-oxopiperazin-1-yl]-4-methyl-N- phenylbenzamide 198 3-[(2R)-4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-2-(hydroxymethyl)piperazin-1-yl]- 4-methyl-N-phenylbenzamide 199 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5-(pyrrolidin-1- ylcarbonyl)-N-(2-pyrrolidin-1-ylethyl)aniline 200 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N,4-dimethyl-5-[(2- pyrrolidin-1-ylethyl)amino]benzamide 201 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N-(4-chlorophenyl)-4- methyl-5-[(2-pyrrolidin-1-ylethyl)amino]benzamide 202 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N-(2-chlorophenyl)-4- methyl-5-[(2-pyrrolidin-1-ylethyl)amino]benzamide 203 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5- [(cyclopropylmethyl)oxy]-2-methyl-N-(2-pyrrolidin-1-ylethyl)aniline 204 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5-[(3- methylbutyl)oxy]-N-(2-pyrrolidin-1-ylethyl)aniline 205 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-[(2-ethylbutyl)oxy]-2- methyl-N-(2-pyrrolidin-1-ylethyl)aniline 206 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-(butyloxy)-2-methyl-N- (2-pyrrolidin-1-ylethyl)aniline 207 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-N-(1- methylethyl)-5-[(2-pyrrolidin-1-ylethyl)amino]benzamide 208 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N,4-dimethyl-N-(1- methylethyl)-5-[(2-pyrrolidin-1-ylethyl)amino]benzamide 209 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5- [(cyclobutylmethyl)oxy]-2-methyl-N-(2-pyrrolidin-1-ylethyl)aniline 210 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-(ethyloxy)-2-methyl-N- (2-pyrrolidin-1-ylethyl)aniline 211 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N-[2- (dimethylamino)ethyl]-4-methylbenzamide 212 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N-(1,1-dimethylethyl)-4- methyl-5-[(2-pyrrolidin-1-ylethyl)amino]benzamide 213 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-N-pyridin-3-yl- 5-[(2-pyrrolidin-1-ylethyl)amino]benzamide 214 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-[(2-fluoro-2- methylpropyl)oxy]-2-methyl-N-(2-pyrrolidin-1-ylethyl)aniline 215 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5- [(cyclohexylmethyl)oxy]-2-methyl-N-(2-pyrrolidin-1-ylethyl)aniline 216 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5- [(cyclopentylmethyl)oxy]-2-methyl-N-(2-pyrrolidin-1-ylethyl)aniline 217 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N-ethyl-4-methyl-5-[(2- pyrrolidin-1-ylethyl)amino]benzamide 218 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5-[(1- methylethyl)oxy]-N-(2-pyrrolidin-1-ylethyl)aniline 219 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-[(2,2- dimethylpropyl)oxy]-2-methyl-N-(2-pyrrolidin-1-ylethyl)aniline 220 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-N-(2- pyrrolidin-1-ylethyl)-5-[(tetrahydrofuran-2-ylmethyl)oxy]aniline 221 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5-{[2- (methyloxy)ethyl]oxy}-N-(2-pyrrolidin-1-ylethyl)aniline 222 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5-(propyloxy)- N-(2-pyrrolidin-1-ylethyl)aniline 223 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-{[2- (dimethylamino)ethyl]amino}-4-methyl-N-phenylbenzamide 224 N′-{3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-[(2-fluoro-2- methylpropyl)oxy]-2-methylphenyl}-N,N-dimethylethane-1,2-diamine 225 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-{[2- (dimethylamino)ethyl]amino}-4-methyl-N-(1-methylethyl)benzamide 226 1-{3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-5-[(2- pyrrolidin-1-ylethyl)amino]phenyl}pentan-1-one 227 N′-(3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-{[2,3-difluoro-2- (fluoromethyl)propyl]oxy}-2-methylphenyl)-N,N-dimethylethane-1,2-diamine 228 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-{[2,3-difluoro-2- (fluoromethyl)propyl]oxy}-2-methyl-N-(2-pyrrolidin-1-ylethyl)aniline 229 5-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-N-(2- pyrrolidin-1-ylethyl)biphenyl-3-amine 230 1-(3-{5-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methylbiphenyl- 3-yl}propyl)pyridinium 231 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-N-(2- pyrrolidin-1-ylethyl)-5-(1,3-thiazol-2-yl)aniline 232 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-5-[(2- pyrrolidin-1-ylethyl)amino]benzoic acid 233 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5- (phenylethynyl)-N-(2-pyrrolidin-1-ylethyl)aniline 234 {3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-5-[(2- pyrrolidin-1-ylethyl)amino]phenyl}(phenyl)methanone 235 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-ethynyl-2-methyl-N-(2- pyrrolidin-1-ylethyl)aniline 236 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-(3,3-dimethylbut-1-yn- 1-yl)-2-methyl-N-(2-pyrrolidin-1-ylethyl)aniline 237 3-bromo-4-{4-[5-{[2,3-difluoro-2-(fluoromethyl)propyl]oxy}-2-methyl-3-(3-pyrrolidin-1- ylpropyl)phenyl]piperazin-1-yl}-1H-pyrazolo[3,4-d]pyrimidine 238 3-bromo-4-{4-[2-methyl-5-[(2-methylpropyl)oxy]-3-(3-pyrrolidin-1- ylpropyl)phenyl]piperazin-1-yl}-1H-pyrazolo[3,4-d]pyrimidine 239 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5-(3-phenyl- 1,2,4-oxadiazol-5-yl)-N-(2-pyrrolidin-1-ylethyl)aniline 240 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5-(3-methyl- 1,2,4-oxadiazol-5-yl)-N-(2-pyrrolidin-1-ylethyl)aniline 241 1-{3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-5-[(2- pyrrolidin-1-ylethyl)amino]phenyl}propan-1-one 242 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-(3,3-dimethylbutyl)-2- methyl-N-(2-pyrrolidin-1-ylethyl)aniline 243 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-ethyl-2-methyl-N-(2- pyrrolidin-1-ylethyl)aniline 244 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-N-(2- pyrrolidin-1-ylethyl)-5-[2-(trimethylsilyl)ethyl]aniline 245 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5-(2- phenylethyl)-N-(2-pyrrolidin-1-ylethyl)aniline 246 1-{3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-5-[(2- pyrrolidin-1-ylethyl)amino]phenyl}butan-1-one 247 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N,4-dimethyl-N- (methyloxy)-5-[(2-pyrrolidin-1-ylethyl)amino]benzamide 248 3-bromo-4-[4-(3-bromo-5-{[2,3-difluoro-2-(fluoromethyl)propyl]oxy}-2- methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 249 4-[4-(3-bromo-5-{[2,3-difluoro-2-(fluoromethyl)propyl]oxy}-2-methylphenyl)piperazin-1- yl]-3-ethyl-1H-pyrazolo[3,4-d]pyrimidine 250 1-{3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-5-[(2- pyrrolidin-1-ylethyl)amino]phenyl}ethanone 251 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-[(difluoromethyl)oxy]- 2-methyl-N-(2-pyrrolidin-1-ylethyl)aniline 252 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5- {[(difluoromethyl)oxy]methyl}-2-methyl-N-(2-pyrrolidin-1-ylethyl)aniline 253 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5-(methyloxy)- N-(2-pyrrolidin-1-ylethyl)aniline 254 5-{[2,3-difluoro-2-(fluoromethyl)propyl]oxy}-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin- 4-yl)piperazin-1-yl]-2-methyl-N-(2-pyrrolidin-1-ylethyl)aniline 255 2-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-3,5,6-trifluoro-N-(3- methylbutyl)pyridin-4-amine 256 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N- [(cyclopropylmethyl)oxy]-4-methyl-5-[(2-pyrrolidin-1-ylethyl)amino]benzamide 257 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5-(5-methyl- 1,2,4-oxadiazol-3-yl)-N-(2-pyrrolidin-1-ylethyl)aniline 258 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-(ethylsulfonyl)-2- methyl-N-(2-pyrrolidin-1-ylethyl)aniline 259 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-5- (methylsulfonyl)-N-(2-pyrrolidin-1-ylethyl)aniline 260 1-{3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-5-[(2- pyrrolidin-1-ylethyl)amino]phenyl}pentan-1-one 261 3-bromo-4-[4-(5-{[2,3-difluoro-2-(fluoromethyl)propyl]oxy}-2-methylphenyl)piperazin-1- yl]-1H-pyrazolo[3,4-d]pyrimidine 262 6-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-3,5-difluoro-N~4~-(3- methylbutyl)-N~2~-(2-pyrrolidin-1-ylethyl)pyridine-2,4-diamine 263 3-bromo-5-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N-(2-pyrrolidin- 1-ylethyl)aniline 264 3-bromo-4-[4-(3′,4′,6-trifluoro-4-methylbiphenyl-3-yl)piperazin-1-yl]-1H-pyrazolo[3,4- d]pyrimidine 265 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-chloro-N-(2-pyrrolidin- 1-ylethyl)aniline 266 {3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-5-[(2- pyrrolidin-1-ylethyl)amino]phenyl}methanol 267 3-bromo-4-(4-{4-methyl-2′-[(2-pyrrolidin-1-ylethyl)oxy]biphenyl-3-yl}piperazin-1-yl)-1H- pyrazolo[3,4-d]pyrimidine 268 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-{[(2,2- difluorocyclopropyl)methyl]oxy}-2-methyl-N-(2-pyrrolidin-1-ylethyl)aniline 269 5-bromo-3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-N-(2- pyrrolidin-1-ylethyl)aniline 270 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-[(ethyloxy)methyl]-2- methyl-N-(2-pyrrolidin-1-ylethyl)aniline 271 3-[4-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-1-methyl-6- (trifluoromethyl)-1H-benzimidazol-2-yl]propan-1-ol 272 1-{3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-5-[(2- pyrrolidin-1-ylethyl)amino]phenyl}-4,4,4-trifluorobutan-1-one 273 {3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-5-[(2- pyrrolidin-1-ylethyl)amino]phenyl}(cyclopropyl)methanone 274 3-({3′-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4′-methylbiphenyl-2- yl}oxy)-N,N-dimethylpropan-1-amine 275 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-(1,1-difluorobutyl)-2- methyl-N-(2-pyrrolidin-1-ylethyl)aniline 276 3-bromo-4-(4-{4-methyl-2′-[(3-morpholin-4-ylpropyl)oxy]biphenyl-3-yl}piperazin-1-yl)- 1H-pyrazolo[3,4-d]pyrimidine 277 3-bromo-4-(4-{4-methyl-2′-[(2-morpholin-4-ylethyl)oxy]biphenyl-3-yl}piperazin-1-yl)-1H- pyrazolo[3,4-d]pyrimidine 278 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-N-(2- pyrrolidin-1-ylethyl)-5-{[(2,2,2-trifluoroethyl)oxy]methyl}aniline 279 1-[2-({3′-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4′- methylbiphenyl-2-yl}oxy)ethyl]pyrrolidine-2,5-dione 280 3-bromo-4-(4-{3′-fluoro-4-methyl-2′-[(2-pyrrolidin-1-ylethyl)oxy]biphenyl-3-yl}piperazin- 1-yl)-1H-pyrazolo[3,4-d]pyrimidine 281 1-{3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-[(2-pyrrolidin-1- ylethyl)amino]phenyl}butan-1-one 282 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-N-(2- pyrrolidin-1-ylethyl)-5-[(3,3,3-trifluoropropyl)oxy]aniline 283 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-N-(2- pyrrolidin-1-ylethyl)-5-[(2,2,2-trifluoroethyl)oxy]aniline 284 1-{3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-4-methyl-5-[(2- pyrrolidin-1-ylethyl)amino]phenyl}butan-1-ol 285 3-bromo-4-(4-{4-chloro-2′-[(2-pyrrolidin-1-ylethyl)oxy]biphenyl-3-yl}piperazin-1-yl)-1H- pyrazolo[3,4-d]pyrimidine 286 3-[4-(4-{5-{[2,3-difluoro-2-(fluoromethyl)propyl]oxy}-2-methyl-3-[(2-pyrrolidin-1- ylethyl)amino]phenyl}piperazin-1-yl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]prop-2-yn-1-ol 287 3-bromo-4-(4-{4-chloro-4′-fluoro-2′-[(2-pyrrolidin-1-ylethyl)oxy]biphenyl-3-yl}piperazin- 1-yl)-1H-pyrazolo[3,4-d]pyrimidine 288 3-bromo-4-(4-{4-methyl-3′-[(2-pyrrolidin-1-ylethyl)oxy]biphenyl-3-yl}piperazin-1-yl)-1H- pyrazolo[3,4-d]pyrimidine 289 (2E)-3-[4-(4-{5-{[2,3-difluoro-2-(fluoromethyl)propyl]oxy}-2-methyl-3-[(2-pyrrolidin-1- ylethyl)amino]phenyl}piperazin-1-yl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]prop-2-enoic acid 290 3-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-methyl-N-(2- pyrrolidin-1-ylethyl)-5-[4,4,4-trifluoro-1,1-bis(methyloxy)butyl]aniline 291 6-(4-phenylpiperazin-1-yl)-9H-purine 292 6-[4-(3-chlorophenyl)piperazin-1-yl]-9H-purine 293 4-(4-phenylpiperazin-1-yl)-7H-pyrrolo[2,3-d]pyrimidine 294 4-[4-(3-chlorophenyl)piperazin-1-yl]-7H-pyrrolo[2,3-d]pyrimidine 295 4-(4-phenylpiperazin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine 296 4-[4-(3-chlorophenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 297 6-[4-(2-chlorophenyl)piperazin-1-yl]-9H-purine 298 6-[4-(2-fluorophenyl)piperazin-1-yl]-9H-purine 299 4-[4-(2-methylphenyl)piperazin-1-yl]-7H-pyrrolo[2,3-d]pyrimidine 300 4-{4-[2-(methyloxy)phenyl]piperazin-1-yl}-7H-pyrrolo[2,3-d]pyrimidine 301 4-{4-[3-(methyloxy)phenyl]piperazin-1-yl}-7H-pyrrolo[2,3-d]pyrimidine 302 4-{4-[4-(methyloxy)phenyl]piperazin-1-yl}-7H-pyrrolo[2,3-d]pyrimidine 303 4-{4-[3-(trifluoromethyl)phenyl]piperazin-1-yl}-7H-pyrrolo[2,3-d]pyrimidine 304 6-{4-[4-(methyloxy)phenyl]piperazin-1-yl}-9H-purine 305 6-{4-[2-(methyloxy)phenyl]piperazin-1-yl}-9H-purine 306 6-[4-(4-chlorophenyl)piperazin-1-yl]-9H-purine 307 6-[4-(4-fluorophenyl)piperazin-1-yl]-9H-purine 308 4-[4-(4-chlorophenyl)piperazin-1-yl]-7H-pyrrolo[2,3-d]pyrimidine 309 4-[4-(2-chlorophenyl)piperazin-1-yl]-7H-pyrrolo[2,3-d]pyrimidine 310 4-[4-(4-fluorophenyl)piperazin-1-yl]-7H-pyrrolo[2,3-d]pyrimidine 311 4-[4-(2-fluorophenyl)piperazin-1-yl]-7H-pyrrolo[2,3-d]pyrimidine 312 6-{4-[3-(trifluoromethyl)phenyl]piperazin-1-yl}-9H-purine 313 6-[4-(2-methylphenyl)piperazin-1-yl]-9H-purine 314 4-{4-[3-(trifluoromethyl)phenyl]piperazin-1-yl}-1H-pyrazolo[3,4-d]pyrimidine 315 4-[4-(2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 316 4-[4-(3-chlorophenyl)piperazin-1-yl]-3-methyl-1H-pyrazolo[3,4-d]pyrimidine 317 3-methyl-4-[4-(2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 318 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 319 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-methyl-1H-pyrazolo[3,4-d]pyrimidine 320 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-methyl-6-phenyl-1H-pyrazolo[3,4- d]pyrimidine 321 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-ethyl-1H-pyrazolo[3,4-d]pyrimidine 322 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-6-methyl-1H-pyrazolo[3,4-d]pyrimidine 323 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-6-ethyl-1H-pyrazolo[3,4-d]pyrimidine 324 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-6-(1-methylethyl)-1H-pyrazolo[3,4- d]pyrimidine 325 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-phenyl-1H-pyrazolo[3,4-d]pyrimidine 326 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-({[2-(methyloxy)ethyl]oxy}methyl)-1H- pyrazolo[3,4-d]pyrimidine 327 3-bromo-4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 328 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-propyl-1H-pyrazolo[3,4-d]pyrimidine 329 4-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-3- yl}phenol 330 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-N-phenyl-1H-pyrazolo[3,4-d]pyrimidin-3- amine 331 4-[4-(3-chlorophenyl)piperazin-1-yl]-3-ethyl-1H-pyrazolo[3,4-d]pyrimidine 332 4-{4-[5-chloro-2-(methyloxy)phenyl]piperazin-1-yl}-3-ethyl-1H-pyrazolo[3,4- d]pyrimidine 333 3-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-3- yl}phenol 334 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-{3-[(phenylmethyl)oxy]phenyl}-1H- pyrazolo[3,4-d]pyrimidine 335 3-(1,3-benzodioxol-5-yl)-4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4- d]pyrimidine 336 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-(2-thienyl)-1H-pyrazolo[3,4-d]pyrimidine 337 3-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-3- yl}aniline 338 3-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-3- yl}benzoic acid 339 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-(4-methylphenyl)-1H-pyrazolo[3,4- d]pyrimidine 340 N-(4-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-3- yl}phenyl)acetamide 341 4-[4-(3-chlorophenyl)-1,4-diazepan-1-yl]-3-ethyl-1H-pyrazolo[3,4-d]pyrimidine 342 4-[5-(3-chlorophenyl)-2,5-diazabicyclo[2.2.1]hept-2-yl]-3-ethyl-1H-pyrazolo[3,4- d]pyrimidine 343 4-(4-{3-chloro-4-[(2-morpholin-4-ylethyl)oxy]phenyl}piperazin-1-yl)-3-ethyl-1H- pyrazolo[3,4-d]pyrimidine 344 methyl 1-(3-chlorophenyl)-4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazine-2- carboxylate 345 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-(3-methylbut-2-en-1-yl)-1H-pyrazolo[3,4- d]pyrimidine 346 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-(trifluoromethyl)-1H-pyrazolo[3,4- d]pyrimidine 347 methyl 4-(3-chlorophenyl)-1-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazine-2- carboxylate 348 4-(4-{3-chloro-4-[(2-piperidin-1-ylethyl)oxy]phenyl}piperazin-1-yl)-3-ethyl-1H- pyrazolo[3,4-d]pyrimidine 349 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-(1-methylethyl)-1H-pyrazolo[3,4- d]pyrimidine 350 1-(3-chlorophenyl)-4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazine-2-carboxylic acid 351 1-(3-chlorophenyl)-4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-N-methylpiperazine-2- carboxamide 352 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-(phenylmethyl)-1H-pyrazolo[3,4- d]pyrimidine 353 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-(2-methylpropyl)-1H-pyrazolo[3,4- d]pyrimidine 354 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-[4-(methyloxy)phenyl]-1H-pyrazolo[3,4- d]pyrimidine 355 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-(4-fluorophenyl)-1H-pyrazolo[3,4- d]pyrimidine 356 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-[4-(phenyloxy)phenyl]-1H-pyrazolo[3,4- d]pyrimidine 357 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-{4-[(piperidin-4-ylmethyl)oxy]phenyl}- 1H-pyrazolo[3,4-d]pyrimidine 358 1-(3-chlorophenyl)-N-[2-(dimethylamino)ethyl]-4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4- yl)piperazine-2-carboxamide 359 4-[4-(5-chloro-2-methyl-3-morpholin-4-ylphenyl)piperazin-1-yl]-3-ethyl-1H-pyrazolo[3,4- d]pyrimidine 360 4-(3-chlorophenyl)-1-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-N-methylpiperazine-2- carboxamide 361 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-[2-(methyloxy)phenyl]-1H-pyrazolo[3,4- d]pyrimidine 362 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-pyridin-4-yl-1H-pyrazolo[3,4- d]pyrimidine 363 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-[3-(methyloxy)phenyl]-1H-pyrazolo[3,4- d]pyrimidine 364 4-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-3- yl}benzonitrile 365 [5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- (methyloxy)phenyl]methanol 366 methyl 5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- (methyloxy)benzoate 367 (2E)-3-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-3- yl}prop-2-enoic acid 368 3-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-3- yl}propanoic acid 369 3-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-3- yl}propan-1-ol 370 methyl (2E)-3-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4- d]pyrimidin-3-yl}prop-2-enoate 371 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-{4-[(2-morpholin-4-ylethyl)oxy]phenyl}- 1H-pyrazolo[3,4-d]pyrimidine 372 5-chloro-N-[2-(dimethylamino)ethyl]-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4- yl)piperazin-1-yl]-2-(methyloxy)benzamide 373 4-(4-{5-chloro-2-(methyloxy)-3-[(4-methylpiperazin-1-yl)carbonyl]phenyl}piperazin-1-yl)- 3-ethyl-1H-pyrazolo[3,4-d]pyrimidine 374 2-(dimethylamino)ethyl 5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4- yl)piperazin-1-yl]-2-(methyloxy)benzoate 375 1-[5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- (methyloxy)phenyl]-N,N-dimethylmethanamine 376 N′-{[5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- (methyloxy)phenyl]methyl}-N,N-dimethylethane-1,2-diamine 377 [1-(3-chlorophenyl)-4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-2-yl]methanol 378 3-[(4-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-3- yl}phenyl)oxy]-N,N-dimethylpropan-1-amine 379 2-chloro-4-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5-methylphenol 380 1-(3-chlorophenyl)-4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-N-(1-methylpiperidin-4- yl)piperazine-2-carboxamide 381 1-(3-chlorophenyl)-4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-N-(2-morpholin-4- ylethyl)piperazine-2-carboxamide 382 2-{[5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- (methyloxy)phenyl]oxy}-N,N-dimethylethanamine 383 3-{5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- methylphenyl}-N,N-dimethylprop-2-yn-1-amine 384 N′-{5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- methylphenyl}-N,N-dimethylethane-1,2-diamine 385 1,1-dimethylethyl (2E)-3-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H- pyrazolo[3,4-d]pyrimidin-3-yl}prop-2-enoate 386 3-({2-chloro-4-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5- methylphenyl}oxy)-N,N-dimethylpropan-1-amine 387 2-({2-chloro-4-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-5- methylphenyl}oxy)-N,N-dimethylethanamine 388 4-{4-[5-chloro-2-methyl-4-(methyloxy)phenyl]piperazin-1-yl}-3-ethyl-1H-pyrazolo[3,4- d]pyrimidine 389 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-(4-methylpiperazin-1-yl)-1H- pyrazolo[3,4-d]pyrimidine 390 3-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-N,N- diethylprop-2-yn-1-amine 391 3-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}prop- 2-yn-1-ol 392 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-(piperidin-4-ylmethyl)-1H-pyrazolo[3,4- d]pyrimidine 393 phenylmethyl (3aR,6aS)-5-({4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H- pyrazolo[3,4-d]pyrimidin-3-yl}methylidene)hexahydrocyclopenta[c]pyrrole-2(1H)- carboxylate 394 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-[(E)-(3aR,6aS)- hexahydrocyclopenta[c]pyrrol-5(1H)-ylidenemethyl]-1H-pyrazolo[3,4-d]pyrimidine 395 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-(3-pyrrolidin-1-ylprop-1-yn-1-yl)-1H- pyrazolo[3,4-d]pyrimidine 396 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-[3-(4-methylpiperazin-1-yl)prop-1-yn-1- yl]-1H-pyrazolo[3,4-d]pyrimidine 397 3-{4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-N,N- diethylpropan-1-amine 398 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-(3-pyrrolidin-1-ylpropyl)-1H- pyrazolo[3,4-d]pyrimidine 399 4-[4-(5-chloro-2-methylphenyl)piperazin-1-yl]-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H- pyrazolo[3,4-d]pyrimidine 400 3-{5-chloro-3-[4-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2- methylphenyl}-N,N-diethylpropan-1-amine 401 4-{4-[5-chloro-2-methyl-3-(3-pyrrolidin-1-ylpropyl)phenyl]piperazin-1-yl}-3-ethyl-1H- pyrazolo[3,4-d]pyrimidine

Table 2b Additional Representative AKT Inhibitors

The Compounds in Table 2b can be prepared as pharmaceutically acceptable salts, solvates, hydrates, and/or isomers thereof. All such salt, solvate, hydrate, and isomer combinations of the Compounds in Table 2b can be used to practice the invention.

Entry Name 1 [1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- chlorophenyl)methanol 2 2-{[[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- chlorophenyl)methyl]oxy}-N,N-dimethylethanamine 3 3-{[[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- chlorophenyl)methyl]oxy}-N,N-dimethylpropan-1-amine 4 3-bromo-4-{4-[(4-bromophenyl)methyl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 5 {4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-1-[(4- chlorophenyl)methyl]piperazin-2-yl}methanol 6 N′-[[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- chlorophenyl)methyl]-N,N-diethylethane-1,2-diamine 7 3-bromo-4-(4-{[4-(1,1-dimethylethyl)phenyl]methyl}piperazin-1-yl)-1H- pyrazolo[3,4-d]pyrimidine 8 4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-1-[(4- chlorophenyl)methyl]piperazin-2-one 9 2-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-2-(4- chlorophenyl)-N-[2-(dimethylamino)ethyl]acetamide 10 N-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl]-N-(4- chlorophenyl)-N′,N′-diethylpropane-1,3-diamine 11 3-bromo-4-(4-{[4-(trifluoromethyl)phenyl]methyl}piperazin-1-yl)-1H- pyrazolo[3,4-d]pyrimidine 12 N-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl]-N-(4- chlorophenyl)-N′-[2-(dimethylamino)ethyl]urea 13 N-[[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- chlorophenyl)methyl]-N′-[2-(dimethylamino)ethyl]urea 14 2-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-2-oxopiperazin-1-yl]-2-(4- chlorophenyl)-N-[2-(dimethylamino)ethyl]acetamide 15 2-(dimethylamino)ethyl [1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4- yl)piperidin-4-yl](4-chlorophenyl)carbamate 16 3-bromo-4-{4-[(4-chloro-3-fluorophenyl)methyl]piperazin-1-yl}-1H- pyrazolo[3,4-d]pyrimidine 17 3-bromo-4-{4-[(4-chloro-2-fluorophenyl)methyl]piperazin-1-yl}-1H- pyrazolo[3,4-d]pyrimidine 18 N-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl]-N-(4- chlorophenyl)-N′,N′-diethylethane-1,2-diamine 19 3-bromo-4-{4-[(4-chlorophenyl)methyl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 20 [1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- fluorophenyl)methanone 21 N-[[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- chlorophenyl)methyl]-N′,N′-diethyl-N-methylethane-1,2-diamine 22 [1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- fluorophenyl)methanol 23 3-bromo-4-(4-{[2-fluoro-4-(trifluoromethyl)phenyl]methyl}piperazin-1-yl)-1H- pyrazolo[3,4-d]pyrimidine 24 N-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl]-N-(4- chlorophenyl)-N~3~,N~3~-diethyl-beta-alaninamide 25 2-{[[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- fluorophenyl)methyl]oxy}-N,N-dimethylethanamine 26 N-[[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- chlorophenyl)methyl]-N~3~,N~3~-diethyl-beta-alaninamide 27 3-bromo-4-{4-[(3,4-dichlorophenyl)methyl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 28 N-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl]-N-(4- chlorophenyl)-N′-[2-(dimethylamino)ethyl]ethanediamide 29 N-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl]-N-(4- chlorophenyl)-2-(diethylamino)ethanesulfonamide 30 4-[4-(biphenyl-4-ylmethyl)piperazin-1-yl]-3-bromo-1H-pyrazolo[3,4- d]pyrimidine 31 3-bromo-4-{(3S)-4-[(4-chlorophenyl)methyl]-3-methylpiperazin-1-yl}-1H- pyrazolo[3,4-d]pyrimidine 32 3-bromo-4-(4-{[4-(methyloxy)phenyl]methyl}piperazin-1-yl)-1H-pyrazolo[3,4- d]pyrimidine 33 4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-N-[3- (trifluoromethyl)phenyl]piperazine-1-carboxamide 34 3-bromo-4-{4-[(4-fluorophenyl)methyl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 35 N-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl]-N-(4- chlorophenyl)pent-4-enamide 36 3-bromo-4-[4-(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)piperazin-1-yl]-1H- pyrazolo[3,4-d]pyrimidine 37 4-[4-(1,3-benzodioxol-5-ylmethyl)piperazin-1-yl]-3-bromo-1H-pyrazolo[3,4- d]pyrimidine 38 [1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- chlorophenyl)methanone 39 3-bromo-4-(4-{[4-(phenyloxy)phenyl]methyl}piperazin-1-yl)-1H-pyrazolo[3,4- d]pyrimidine 40 3-bromo-4-{4-[(3,4-dichlorophenyl)methyl]piperidin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 41 4-{[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]methyl}-N,N- dimethylaniline 42 methyl 4-{[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1- yl]methyl}benzoate 43 3-bromo-4-{4-[(2E)-3-phenylprop-2-enoyl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 44 1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-4-[(4-chlorophenyl)methyl]-N- [3-(diethylamino)propyl]piperidine-4-carboxamide 45 3-bromo-4-{4-[(2-bromophenyl)methyl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 46 3-bromo-4-{4-[(2-chlorophenyl)methyl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 47 3-bromo-4-{4-[(2,4-dichlorophenyl)methyl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 48 3-bromo-4-{4-[(2-chloro-4-fluorophenyl)methyl]piperazin-1-yl}-1H- pyrazolo[3,4-d]pyrimidine 49 1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-4-(4-chlorophenyl)-N-[3- (diethylamino)propyl]piperidine-4-carboxamide 50 3-bromo-4-[4-(phenylmethyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 51 2-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N-pyridin-2- ylacetamide 52 3-bromo-4-[4-(1H-imidazol-2-ylmethyl)piperazin-1-yl]-1H-pyrazolo[3,4- d]pyrimidine 53 3-bromo-4-(4-{[3-(phenyloxy)phenyl]methyl}piperazin-1-yl)-1H-pyrazolo[3,4- d]pyrimidine 54 3-bromo-4-{4-[(3-methylphenyl)methyl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 55 3-{[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1- yl]methyl}benzonitrile 56 3-bromo-4-{4-[(2-chloro-6-fluorophenyl)methyl]piperazin-1-yl}-1H- pyrazolo[3,4-d]pyrimidine 57 3-bromo-4-[4-(1-phenylethyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 58 3-bromo-4-[4-(pyridin-4-ylmethyl)piperazin-1-yl]-1H-pyrazolo[3,4- d]pyrimidine 59 1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-N-(4-chlorophenyl)piperidin-4- amine 60 3-bromo-4-[4-(pyridin-3-ylmethyl)piperazin-1-yl]-1H-pyrazolo[3,4- d]pyrimidine 61 3-bromo-4-(4-{[2,3,4-tris(methyloxy)phenyl]methyl}piperazin-1-yl)-1H- pyrazolo[3,4-d]pyrimidine 62 3-bromo-4-[4-({3-[(phenylmethyl)oxy]phenyl}methyl)piperazin-1-yl]-1H- pyrazolo[3,4-d]pyrimidine 63 3-bromo-4-[4-(naphthalen-1-ylmethyl)piperazin-1-yl]-1H-pyrazolo[3,4- d]pyrimidine 64 3-bromo-4-(4-{[5-(4-chlorophenyl)furan-2-yl]methyl}piperazin-1-yl)-1H- pyrazolo[3,4-d]pyrimidine 65 3-bromo-4-[4-({4-[(4-fluorophenyl)oxy]-3-nitrophenyl}methyl)piperazin-1-yl]- 1H-pyrazolo[3,4-d]pyrimidine 66 3-bromo-4-[4-(furan-2-ylcarbonyl)piperazin-1-yl]-1H-pyrazolo[3,4- d]pyrimidine 67 3-bromo-4-[4-(1H-indol-6-ylcarbonyl)piperazin-1-yl]-1H-pyrazolo[3,4- d]pyrimidine 68 3-bromo-4-{4-[2-(2-thienyl)ethyl]piperazin-1-yl}-1H-pyrazolo[3,4-d]pyrimidine 69 3-bromo-4-[4-(3-pyrrolidin-1-ylpropyl)piperazin-1-yl]-1H-pyrazolo[3,4- d]pyrimidine 70 3-bromo-4-[4-(cyclohexylmethyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 71 3-bromo-4-{4-[(10-chloroanthracen-9-yl)methyl]piperazin-1-yl}-1H- pyrazolo[3,4-d]pyrimidine 72 3-bromo-4-[4-(1-methylpropyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidine 73 4-(4-{[4,6-bis(methyloxy)pyrimidin-2-yl]methyl}piperazin-1-yl)-3-bromo-1H- pyrazolo[3,4-d]pyrimidine 74 3-bromo-4-{4-[2-(methyloxy)ethyl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 75 3-bromo-4-[4-(2-morpholin-4-yl-2-oxoethyl)piperazin-1-yl]-1H-pyrazolo[3,4- d]pyrimidine 76 3-bromo-4-{4-[3-(methyloxy)propyl]piperazin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 77 4-{4-[[4,6-bis(methyloxy)pyrimidin-2-yl](phenyl)methyl]piperazin-1-yl}-3- bromo-1H-pyrazolo[3,4-d]pyrimidine 78 3-bromo-4-[4-(6,7,8,9-tetrahydro-5H-benzocyclohepten-5-yl)piperazin-1-yl]- 1H-pyrazolo[3,4-d]pyrimidine 79 3-bromo-4-[4-({4-[(phenylmethyl)oxy]phenyl}methyl)piperazin-1-yl]-1H- pyrazolo[3,4-d]pyrimidine 80 3-bromo-4-[4-({3-chloro-4-[(phenylmethyl)oxy]phenyl}methyl)piperazin-1-yl]- 1H-pyrazolo[3,4-d]pyrimidine 81 4-{[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]methyl}-N-(3- morpholin-4-ylpropyl)benzamide 82 4-{[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]methyl}-N-[3- (methyloxy)propyl]benzamide 83 2-[({4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-1-[(4- chlorophenyl)methyl]piperazin-2-yl}methyl)oxy]-N,N-dimethylethanamine 84 3-bromo-4-[4-({4-[(4-chlorophenyl)oxy]-3-nitrophenyl}methyl)piperazin-1-yl]- 1H-pyrazolo[3,4-d]pyrimidine 85 2-[4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl]-N,N- dimethylacetamide 86 2-{[(R)-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- chlorophenyl)methyl]oxy}-N,N-dimethylethanamine 87 N-(4-bromo-3-fluorophenyl)-N-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4- yl)piperidin-4-yl]-N′-[2-(dimethylamino)ethyl]urea 88 2-({(R)-(4-chlorophenyl)[1-(3-ethyl-1H-pyrazolo[3,4-d]pyrimidin-4- yl)piperidin-4-yl]methyl}oxy)-N,N-dimethylethanamine 89 2-{[(S)-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- chlorophenyl)methyl]oxy}-N,N-dimethylethanamine 90 3-bromo-4-(4-{(R)-(4-chlorophenyl)[(2-pyrrolidin-1- ylethyl)oxy]methyl}piperidin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine 91 1-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl]-1-(4- chlorophenyl)-4-(dimethylamino)butan-1-ol 92 2-{[(R)-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- chloro-3-fluorophenyl)methyl]oxy}-N,N-dimethylethanamine 93 3-bromo-4-(4-{(R)-(4-chlorophenyl)[(2-piperidin-1- ylethyl)oxy]methyl}piperidin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine 94 4-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl]-4-(4- chlorophenyl)-N,N-dimethylbutan-1-amine 95 3-bromo-4-(4-{(R)-(4-chlorophenyl)[(2-morpholin-4- ylethyl)oxy]methyl}piperidin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine 96 1-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl]-1-(4- fluorophenyl)-N-(furan-2-ylmethyl)-N-methylmethanamine 97 1-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl]-1-(4- fluorophenyl)-N-methyl-N-(pyridin-2-ylmethyl)methanamine 98 4-{[{[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- fluorophenyl)methyl}(methyl)amino]methyl}-N,N-dimethylaniline 99 [4-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperazin-1-yl](1H-indol-6- yl)methanol 100 3-bromo-4-(4-{(R)-(4-chloro-3-fluorophenyl)[(2-pyrrolidin-1- ylethyl)oxy]methyl}piperidin-1-yl)-1H-pyrazolo[3,4-d]pyrimidine 101 3-bromo-4-{4-[(4-chlorophenyl)oxy]piperidin-1-yl}-1H-pyrazolo[3,4- d]pyrimidine 102 2-{[(R)-[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl](4- chlorophenyl)methyl]oxy}-N,N-diethylethanamine 103 2-{[1-(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidin-4-yl]oxy}-5- chloro-N-(2-pyrrolidin-1-ylethyl)aniline

Table 3a Representative c-MET and/or Flt-3 Inhibitors

The Compounds in Table 3a can be prepared as pharmaceutically acceptable salts, solvates, hydrates, and/or isomers thereof. All such salt, solvate, hydrate, and isomer combinations of the Compounds in Table 3a can be used to practice the invention.

Cmpd No. Name 1 N-(4-fluorophenyl)-N′-[3-fluoro-4-(7H-pyrrolo[2,3- d]pyrimidin-4-yloxy)phenyl]propanediamide 2 N-(4-fluorophenyl)-N′-[3-fluoro-4-(7H-pyrrolo[2,3- d]pyrimidin-4-yloxy)phenyl]cyclopropane-1,1-dicarboxamide 3 N-({[3-fluoro-4-(7H-pyrrolo[2,3-d]pyrimidin-4- yloxy)phenyl]amino}carbonothioyl)-2-phenylacetamide 4 N-(4-fluorophenyl)-N′-(4-{[1-(tetrahydro-2H-pyran-2-yl)-1H- pyrazolo[3,4-d]pyrimidin-4-yl]oxy}phenyl)cyclopropane-1,1- dicarboxamide 5 2-phenyl-N-{[(4-{[1-(tetrahydro-2H-pyran-2-yl)-1H- pyrazolo[3,4-d]pyrimidin-4- yl]oxy}phenyl)amino]carbonothioyl}acetamide 6 N-(4-fluorophenyl)-N′-[4-(1H-pyrazolo[3,4-d]pyrimidin-4- yloxy)phenyl]cyclopropane-1,1-dicarboxamide 7 2-phenyl-N-({[4-(1H-pyrazolo[3,4-d]pyrimidin-4- yloxy)phenyl]amino}carbonothioyl)acetamide 8 N-(4-fluorophenyl)-N′-(4-{[9-(tetrahydro-2H-pyran-2-yl)-9H- purin-6-yl]oxy}phenyl)cyclopropane-1,1-dicarboxamide 9 2-phenyl-N-{[(4-{[9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6- yl]oxy}phenyl)amino]carbonothioyl}acetamide 10 N-(4-fluorophenyl)-N′-[4-(9H-purin-6- yloxy)phenyl]cyclopropane-1,1-dicarboxamide 11 2-phenyl-N-({[4-(9H-purin-6- yloxy)phenyl]amino}carbonothioyl)acetamide 12 N-{3-fluoro-4-[(6-{[(2-morpholin-4-ylethyl)amino]carbonyl}- 7H-pyrrolo[2,3-d]pyrimidin-4-yl)oxy]phenyl}-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide

Table 3b Additional Representative c-MET, c-KIT, and/or Flt-3 Inhibitors

The Compounds in Table 3b can be prepared as pharmaceutically acceptable salts, solvates, hydrates, and/or isomers thereof. All such salt, solvate, hydrate, and isomer combinations of the Compounds in Table 3b can be used to practice the invention.

Entry Name 1 N-[({3-fluoro-4-[(6-(methyloxy)-7-{[(3aR,6aS)- octahydrocyclopenta[c]pyrrol-5-ylmethyl]oxy}quinazolin-4- yl)oxy]phenyl}amino)carbonothioyl]-2-phenylacetamide 2 N-{[(3-fluoro-4-{[7-({[(3aR,6aS)-2-methyloctahydrocyclopenta[c]pyrrol- 5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4- yl]oxy}phenyl)amino]carbonothioyl}-2-phenylacetamide 3 N-{[(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3- fluorophenyl)(methyl)amino]carbonothioyl}-2-phenylacetamide 4 1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)imidazolidin-2-one 5 1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-3- (phenylmethyl)imidazolidin-2-one 6 1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-3- (phenylacetyl)imidazolidin-2-one 7 ethyl [(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3- fluorophenyl)amino](oxo)acetate 8 N-{[(4-{[6,7-bis(methyloxy)quinazolin-4-yl]amino}-3- fluorophenyl)amino]carbonothioyl}-2-phenylacetamide 9 N′-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N-methyl- N-(2-phenylethyl)sulfamide 10 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-3- (phenylmethyl)-1,2,4-oxadiazol-5-amine 11 1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)piperidin-2- one 12 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′- (phenylmethyl)ethanediamide 13 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-4-phenyl- 1,3-thiazol-2-amine 14 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-(2- phenylethyl)ethanediamide 15 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-1- phenylmethanesulfonamide 16 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-2- phenylethanesulfonamide 17 4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluoro-N- (phenylmethyl)benzenesulfonamide 18 4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluoro-N-methyl-N- (phenylmethyl)benzenesulfonamide 19 4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluoro-N-(2- phenylethyl)benzenesulfonamide 20 4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluoro-N-methyl-N-(2- phenylethyl)benzenesulfonamide 21 4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluoro-N-(3- phenylpropyl)benzenesulfonamide 22 1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)pyrrolidin-2- one 23 4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl (phenylmethyl)carbamate 24 4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl (2-phenylethyl)carbamate 25 4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluoro-N-methyl-N-(3- phenylpropyl)benzenesulfonamide 26 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′- phenylethanediamide 27 N-{[(3-fluoro-4-{[7-{[(2-methyloctahydrocyclopenta[c]pyrrol-5- yl)methyl]oxy}-6-(methyloxy)quinolin-4- yl]oxy}phenyl)amino]carbonothioyl}-2-phenylacetamide 28 N-[(Z)-[(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3- fluorophenyl)amino](imino)methyl]-2-phenylacetamide 29 4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluoro-N-[2- (phenyloxy)ethyl]benzenesulfonamide 30 N,N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-bis-(3- phenylpropane-1-sulfonamide) 31 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-3- phenylpropane-1-sulfonamide 32 N2-[(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)sulfonyl]- N1-phenylglycinamide 33 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}pyridin-3-yl)-2- phenylacetamide 34 N-{[(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}pyridin-3- yl)amino]carbonothioyl}-2-phenylacetamide 35 6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-1,3-benzothiazol-2-amine 36 6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-fluoro-1,3-benzothiazol-2- amine 37 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-fluoro-1,3-benzothiazol-2- yl)-2-phenylacetamide 38 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-(2- morpholin-4-ylethyl)ethanediamide 39 benzyl-{[4-(6,7-dimethoxy-quinolin-4-yloxy)-3-fluoro-phenylcarbamoyl]- methyl}-carbamic acid tert-butyl ester 40 N1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N2- (phenylmethyl)glycinamide 41 N2-acetyl-N1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)- N2-(phenylmethyl)glycinamide 42 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-1,3-benzothiazol-2-yl)-2- phenylacetamide 43 benzyl-{[6-(6,7-dimethoxy-quinolin-4-yloxy)-pyridin-3-ylcarbamoyl]- methyl}-carbamic acid tert-butyl ester 44 N1-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}pyridin-3-yl)-N2- (phenylmethyl)glycinamide 45 N2-acetyl-N1-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}pyridin-3-yl)-N2- (phenylmethyl)glycinamide 46 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}pyridin-3-yl)-3- phenylpropanamide 47 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}pyridin-3-yl)-4- phenylbutanamide 48 N1-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}pyridin-3-yl)-N2-methyl- N2-(phenylmethyl)glycinamide 49 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-{2-[4- (methyloxy)phenyl]ethyl}ethanediamide 50 N1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N2- methyl-N2-(phenylmethyl)glycinamide 51 4-[(2-amino-1,3-benzothiazol-6-yl)oxy]-6,7-bis(methyloxy)-1-(2-oxo-2- phenylethyl)quinolinium 52 N-{[(4-{[6,7-bis(methyloxy)quinolin-4- yl]amino}phenyl)amino]carbonothioyl}-2-phenylacetamide 53 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-fluoro-1,3-benzothiazol-2- yl)-3-phenylpropanamide 54 N-{[(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3- yl)amino]carbonothioyl}-2-phenylacetamide 55 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-(2,3- dihydro-1H-inden-1-yl)ethanediamide 56 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-(2,3- dihydro-1H-inden-2-yl)ethanediamide 57 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-(1,2,3,4- tetrahydronaphthalen-1-yl)ethanediamide 58 N′-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N-(2- phenylethyl)-N-(phenylmethyl)sulfamide 59 N1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N2- (trifluoroacetyl)glycinamide 60 N-{[4-(6,7-dimethoxy-quinolin-4-yloxy)-3-fluoro-phenylcarbamoyl]- methyl}-benzamide 61 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}pyridin-3-yl)-N′-(4- fluorophenyl)propanediamide 62 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-[(2S)- 1,2,3,4-tetrahydronaphthalen-2-yl]ethanediamide 63 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-[2-(4- methylphenyl)ethyl]ethanediamide 64 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-(2- phenylpropyl)ethanediamide 65 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-[2-(4- chlorophenyl)ethyl]ethanediamide 66 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N,N′- bis(phenylmethyl)sulfamide 67 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N,N′-bis(2- phenylethyl)sulfamide 68 ethyl [(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3- yl)amino](oxo)acetate 69 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3-yl)-N′-(2- phenylethyl)ethanediamide 70 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3-yl)-N′-(4- fluorophenyl)propanediamide 71 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-(1,2,3,4- tetrahydronaphthalen-2-yl)ethanediamide 72 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-[2-(1- methylpyrrolidin-2-yl)ethyl]ethanediamide 73 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-[2- (phenyloxy)ethyl]ethanediamide 74 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-[2- hydroxy-1-(phenylmethyl)ethyl]urea 75 1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-3-[(4- methylphenyl)sulfonyl]-4-(phenylmethyl)imidazolidin-2-one 76 N′-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N-methyl- N-(2-phenylethyl)ethanediamide 77 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-{[3- (trifluoromethyl)phenyl]methyl}ethanediamide 78 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-{2-[3- (trifluoromethyl)phenyl]ethyl}ethanediamide 79 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3-yl)-3-oxo- 4-phenylbutanamide 80 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3-yl)-2-[3- (trifluoromethyl)phenyl]acetamide 81 6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-fluoro-N-[2- (phenyloxy)ethyl]-1,3-benzothiazol-2-amine 82 6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-fluoro-N-(2-piperidin-1- ylethyl)-1,3-benzothiazol-2-amine 83 6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-fluoro-N-methyl-N-(2- phenylethyl)-1,3-benzothiazol-2-amine 84 6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-fluoro-N-(2-pyrrolidin-1- ylethyl)-1,3-benzothiazol-2-amine 85 6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-fluoro-N-{[3- (trifluoromethyl)phenyl]methyl}-1,3-benzothiazol-2-amine 86 6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-fluoro-N-{2-[3- (trifluoromethyl)phenyl]ethyl}-1,3-benzothiazol-2-amine 87 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3-yl)-N′-[3- (trifluoromethyl)phenyl]propanediamide 88 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-fluoro-1,3-benzothiazol-2- yl)-2-[3-(trifluoromethyl)phenyl]acetamide 89 N1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N2-{[3- (trifluoromethyl)phenyl]methyl}glycinamide 90 N1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N2-(2- phenylethyl)glycinamide 91 N1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N2-{2-[3- (trifluoromethyl)phenyl]ethyl}glycinamide 92 benzyl-{[5-chloro-6-(6,7-dimethoxy-quinolin-4-yloxy)-pyridin-3- ylcarbamoyl]-methyl}-carbamic acid tert-butyl ester 93 N1-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3-yl)-N2- (phenylmethyl)glycinamide 94 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-fluoro-1,3-benzothiazol-2- yl)-2-[3,5-bis(trifluoromethyl)phenyl]acetamide 95 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-fluoro-1,3-benzothiazol-2- yl)-2-[2-chloro-5-(trifluoromethyl)phenyl]acetamide 96 N-{3-fluoro-4-[(6-(methyloxy)-7-{[(1-methylpiperidin-4- yl)methyl]oxy}quinolin-4-yl)oxy]phenyl}-N′-(2- phenylethyl)ethanediamide 97 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-(1,2,3,4- tetrahydroisoquinolin-1-ylmethyl)ethanediamide 98 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-[(2- methyl-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl]ethanediamide 99 N1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N2- methyl-N2-{[3-(trifluoromethyl)phenyl]methyl}glycinamide 100 N1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N2- methyl-N2-{2-[3-(trifluoromethyl)phenyl]ethyl}glycinamide 101 N1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N2- methyl-N2-(2-phenylethyl)glycinamide 102 1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-4- (phenylmethyl)imidazolidin-2-one 103 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}pyridazin-3-yl)-N′-(4- fluorophenyl)propanediamide 104 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3-yl)-N′-(2- chlorophenyl)propanediamide 105 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3-yl)-N′-(3- chlorophenyl)propanediamide 106 N1-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3-yl)-N2- methyl-N2-(phenylmethyl)glycinamide 107 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3-yl)-N′-(4- chlorophenyl)propanediamide 108 (2E)-N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-2- [(methyloxy)imino]propanamide 109 (2E)-N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-2- [(ethyloxy)imino]propanamide 110 (2E)-N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-2- {[(phenylmethyl)oxy]imino}propanamide 111 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-1- (phenylmethyl)prolinamide 112 1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-3-[(4- methylphenyl)sulfonyl]-4-(phenylmethyl)imidazolidin-2-one 113 1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-4- (phenylmethyl)imidazolidin-2-one 114 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-4-(phenylmethyl)- 4,5-dihydro-1,3-oxazol-2-amine 115 6,7-bis(methyloxy)-4-({4-[4-(phenylmethyl)piperazin-1- yl]phenyl}oxy)quinoline 116 1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-4- (phenylmethyl)piperazin-2-one 117 N1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N2- (phenylmethyl)alaninamide 118 N1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N2-methyl-N2- (phenylmethyl)alaninamide 119 N1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N2- (phenylmethyl)leucinamide 120 N1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N2-methyl-N2- (phenylmethyl)leucinamide 121 N1-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N2- (phenylmethyl)valinamide 122 4-(6,7-dimethoxy-quinolin-4-ylamino)-N-(3-phenyl-propyl)-benzamide 123 4-benzyl-1-[4-(6,7-dimethoxy-quinolin-4-yloxy)-phenyl]-tetrahydro- pyrimidin-2-one 124 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-phenethyl-oxalamide 125 2-(Benzyl-methyl-amino)-N-[4-(6,7-dimethoxy-quinolin-4-yloxy)-phenyl]- 3-methyl-butyramide (note: Alphabetic order of prefixes ignored while selecting parent chain) 126 N-[4-(6,7-Dimethoxy-quinolin-4-yloxy)-phenyl]-2-phenoxyimino- propionamide 127 2-Benzyloxyimino-N-[4-(6,7-dimethoxy-quinolin-4-yloxy)-phenyl]-2- phenyl-acetamide 128 4-[4-(4-Benzyl-piperidin-1-yl)-phenoxy]-6,7-dimethoxy-quinoline 129 N-[4-(6,7-Dimethoxy-quinolin-4-yloxy)-3-fluoro-phenyl]-N′-(2-isopropyl- 1,2,3,4-tetrahydro-isoquinolin-1-ylmethyl)-oxalamide 130 N-[4-(6,7-Dimethoxy-quinolin-4-yloxy)-3-fluoro-phenyl]-N′-(2-ethyl- 1,2,3,4-tetrahydro-isoquinolin-1-ylmethyl)-oxalamide 131 4-(4-{3-Chloro-5-[2-(4-fluoro-phenylcarbamoyl)-acetylamino]-pyridin-2- yloxy}-6-methoxy-quinolin-7-yloxymethyl)-piperidine-1-carboxylic acid tert-butyl ester 132 N-{5-Chloro-6-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- pyridin-3-yl}-N′-(4-fluoro-phenyl)-malonamide 133 N-{5-Chloro-6-[6-methoxy-7-(1-methyl-piperidin-4-ylmethoxy)-quinolin- 4-yloxy]-pyridin-3-yl}-N′-(4-fluoro-phenyl)-malonamide 134 N-{4-[7-(3-Diethylamino-propoxy)-6-methoxy-quinolin-4-yloxy]-3-fluoro- phenyl}-N′-phenethyl-oxalamide 135 N-{3-Fluoro-4-[6-methoxy-7-(3-morpholin-4-yl-propoxy)-quinolin-4- yloxy]-phenyl}-N′-phenethyl-oxalamide 136 N-{3-Fluoro-4-[6-methoxy-7-(3-piperidin-1-yl-propoxy)-quinolin-4- yloxy]-phenyl}-N′-phenethyl-oxalamide 137 N-{4-[7-(2-Diethylamino-ethoxy)-6-methoxy-quinolin-4-yloxy]-3-fluoro- phenyl}-N′-phenethyl-oxalamide 138 N-{3-Fluoro-4-[6-methoxy-7-(1-methyl-piperidin-4-ylmethoxy)-quinolin- 4-yloxy]-phenyl}-N′-methyl-N′-phenethyl-oxalamide 139 N-{3-Fluoro-4-[6-methoxy-7-(2-methyl-octahydro-cyclopenta[c]pyrrol-5- ylmethoxy)-quinolin-4-yloxy]-phenyl}-N′-phenethyl-oxalamide 140 N-{3-Fluoro-4-[6-methoxy-7-(2-methyl-octahydro-cyclopenta[c]pyrrol-5- ylmethoxy)-quinazolin-4-yloxy]-phenyl}-N′-phenethyl-oxalamide 141 2-(3,4-Dihydro-1H-isoquinolin-2-yl)-N-{3-fluoro-4-[6-methoxy-7-(1- methyl-piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-2-oxo- acetamide 142 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-2-oxo-2-(3-phenyl-pyrrolidin-1-yl)-acetamide 143 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-2-oxo-2-(2-phenyl-morpholin-4-yl)-acetamide 144 N-(2-Dimethylamino-2-phenyl-ethyl)-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 145 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-oxo-2-phenyl-ethyl)-oxalamide 146 N-[5-Chloro-6-(6,7-dimethoxy-quinolin-4-yloxy)-pyridin-3-yl]-2,2- difluoro-N′-(4-fluoro-phenyl)-malonamide 147 N-Benzyl-N′-{3-fluoro-4-[6-methoxy-7-(1-methyl-piperidin-4-ylmethoxy)- quinolin-4-yloxy]-phenyl}-oxalamide 148 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-[2-(2-fluoro-phenyl)-ethyl]-oxalamide 149 N-[2-(3-Chloro-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 150 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-[2-(2-methoxy-phenyl)-ethyl]-oxalamide 151 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-pyridin-3-yl-ethyl)-oxalamide 152 N-Benzyl-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin- 4-yloxy]-phenyl}-oxalamide 153 N-[2-(2,5-Dimethoxy-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 154 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-[2-(2-trifluoromethyl-phenyl)-ethyl]-oxalamide 155 N-[2-(2-Ethoxy-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 156 N-[2-(2,4-Dimethyl-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 157 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(1S-phenyl-2-p-tolyl-ethyl)-oxalamide 158 N-[2-(4-Chloro-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 159 N-{3-Fluoro-4-[6-methoxy-7-(1-methyl-piperidin-4-ylmethoxy)-quinolin- 4-yloxy]-phenyl}-oxalamic acid 160 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-[2-(3-fluoro-phenyl)-ethyl]-oxalamide 161 N-[2-(2-Chloro-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 162 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-[2-(3-methoxy-phenyl)-ethyl]-oxalamide 163 N-(1,2-Diphenyl-ethyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 164 N-[2-(2,4-Dichloro-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin- 4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 165 N-[2-(3,4-Dimethoxy-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 166 N-[2-(4-Ethyl-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 167 N-[2-(4-Ethoxy-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 168 N-[2-(4-Ethoxy-3-methoxy-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 169 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-[2-(4-phenoxy-phenyl)-ethyl]-oxalamide 170 N-[2-(3-Ethoxy-4-methoxy-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 171 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-pyridin-2-yl-ethyl)-oxalamide 172 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-pyridin-4-yl-ethyl)-oxalamide 173 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-[2-(4-fluoro-phenyl)-ethyl]-oxalamide 174 N-[2-(2-Bromo-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 175 N-[2-(2-Chloro-6-fluoro-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 176 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2R-phenyl-propyl)-oxalamide 177 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-indan-1-yl-oxalamide 178 N-{3-Fluoro-4-[6-methoxy-7-(1-methyl-piperidin-4-ylmethoxy)-quinolin- 4-yloxy]-phenyl}-N′-isobutyl-oxalamide 179 N-{3-Fluoro-4-[6-methoxy-7-(1-methyl-piperidin-4-ylmethoxy)-quinolin- 4-yloxy]-phenyl}-N′-(3-methyl-butyl)-oxalamide 180 N-{3-Fluoro-4-[6-methoxy-7-(1-methyl-piperidin-4-ylmethoxy)-quinolin- 4-yloxy]-phenyl}-N′-(2R-phenyl-propyl)-oxalamide 181 N-{3-Fluoro-4-[6-methoxy-7-(1-methyl-piperidin-4-ylmethoxy)-quinolin- 4-yloxy]-phenyl}-N′-(2-phenyl-propyl)-oxalamide 182 N-{3-Fluoro-4-[6-methoxy-7-(1-methyl-piperidin-4-ylmethoxy)-quinolin- 4-yloxy]-phenyl}-N′-indan-2-yl-oxalamide 183 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(1R-phenyl-ethyl)-oxalamide 184 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(1S-phenyl-ethyl)-oxalamide 185 N-[2-(3-Bromo-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 186 N-[2-(2,6-Dichloro-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin- 4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 187 N-[2-(2,4-Dichloro-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin- 4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 188 N-(2-Benzo[1,3]dioxol-5-yl-ethyl)-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 189 N-[2-(3-Bromo-4-methoxy-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 190 N-[2-(3,5-Dimethoxy-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 191 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-o-tolyl-ethyl)-oxalamide 192 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-m-tolyl-ethyl)-oxalamide 193 N-[2-(3-Ethoxy-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 194 N-[2-(3,4-Dimethyl-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 195 N-[2-(2,5-Dimethyl-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 196 N-[2-(3-Chloro-4-propoxy-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 197 N-[2-(4-Butoxy-3-chloro-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 198 N-[2-(4-tert-Butyl-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin- 4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 199 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-[2-(4-sulfamoyl-phenyl)-ethyl]-oxalamide 200 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-[2-(4-hydroxy-3-methoxy-phenyl)-ethyl]-oxalamide 201 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-[2-(3-hydroxy-4-methoxy-phenyl)-ethyl]-oxalamide 202 N-(2,4-Dichloro-benzyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 203 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(4-fluoro-2-trifluoromethyl-benzyl)-oxalamide 204 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(1-p-tolyl-ethyl)-oxalamide 205 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(3-fluoro-4-trifluoromethyl-benzyl)-oxalamide 206 N-(3-Chloro-4-fluoro-benzyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 207 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-[1-(3-methoxy-phenyl)-ethyl]-oxalamide 208 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(1-naphthalen-2-yl-ethyl)-oxalamide 209 N-(4-Chloro-3-trifluoromethyl-benzyl)-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 210 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(1-p-tolyl-ethyl)-oxalamide 211 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(6-trifluoromethyl-pyridin-3-ylmethyl)-oxalamide 212 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-methyl-benzyl)-oxalamide 213 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(3-methyl-benzyl)-oxalamide 214 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(4-fluoro-3-trifluoromethyl-benzyl)-oxalamide 215 N-(3,5-Dichloro-benzyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 216 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(1R,2,3,4-tetrahydro-naphthalen-1-yl)-oxalamide 217 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(1S,2,3,4-tetrahydro-naphthalen-1-yl)-oxalamide 218 N-Cyclopentyl-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)- quinolin-4-yloxy]-phenyl}-oxalamide 219 N-[1-(4-Bromo-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 220 N-(2-Fluoro-benzyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 221 N-[2-(3,4-Dichloro-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin- 4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 222 N-(4-Fluoro-benzyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 223 N-(2,3-Difluoro-benzyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 224 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-phenoxy-ethyl)-oxalamide 225 N-(2,2-Diphenyl-ethyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 226 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-[2-(4-methoxy-phenyl)-ethyl]-oxalamide 227 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-phenyl-propyl)-oxalamide 228 N-[2-(4-Bromo-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 229 N-{4-[7-(1-Ethyl-piperidin-4-ylmethoxy)-6-methoxy-quinolin-4-yloxy]-3- fluoro-phenyl}-2-oxo-2-(2-phenyl-morpholin-4-yl)-acetamide 230 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(3-fluoro-5-trifluoromethyl-benzyl)-oxalamide 231 N-(3,5-Difluoro-benzyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 232 N-(2-Chloro-5-trifluoromethyl-benzyl)-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 233 N-[4-(6,7-Dimethoxy-quinolin-4-yloxy)-3-fluoro-phenyl]-N′-(2- dimethylamino-2-phenyl-ethyl)-oxalamide 234 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(4-methoxy-benzyl)-oxalamide 235 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(4-trifluoromethyl-benzyl)-oxalamide 236 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(3-methoxy-benzyl)-oxalamide 237 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(3-trifluoromethyl-benzyl)-oxalamide 238 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(3-trifluoromethoxy-benzyl)-oxalamide 239 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-methoxy-benzyl)-oxalamide 240 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-trifluoromethyl-benzyl)-oxalamide 241 N-(3-Chloro-benzyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 242 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-trifluoromethoxy-benzyl)-oxalamide 243 N-(2-Chloro-benzyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 244 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(4-trifluoromethoxy-benzyl)-oxalamide 245 N-{3-Fluoro-4-[6-methoxy-7-(1-methyl-piperidin-4-ylmethoxy)-quinolin- 4-yloxy]-phenyl}-N′-(4-methoxy-benzyl)-oxalamide 246 N-{3-Fluoro-4-[6-methoxy-7-(1-methyl-piperidin-4-ylmethoxy)-quinolin- 4-yloxy]-phenyl}-N′-(4-trifluoromethyl-benzyl)-oxalamide 247 N-{4-[7-(Azetidin-3-ylmethoxy)-6-methoxy-quinolin-4-yloxy]-3-fluoro- phenyl}-N′-phenethyl-oxalamide 248 N-{3-Fluoro-4-[6-methoxy-7-(1-methyl-azetidin-3-ylmethoxy)-quinolin-4- yloxy]-phenyl}-N′-phenethyl-oxalamide 249 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-hydroxy-2-phenyl-ethyl)-oxalamide 250 N-[5-Chloro-6-(6,7-dimethoxy-quinolin-4-yloxy)-pyridin-3-yl]-N′-(2,4- difluoro-phenyl)-malonamide 251 N-[5-Chloro-6-(6,7-dimethoxy-quinolin-4-yloxy)-pyridin-3-yl]-N′-(4- fluoro-phenyl)-N′-methyl-malonamide 252 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(1R-phenyl-propyl)-oxalamide 253 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(1R-phenyl-propyl)-oxalamide 254 N-(3,4-Difluoro-benzyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 255 N-(2,6-Difluoro-benzyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 256 N-{3-Fluoro-4-[6-methoxy-7-(1-methyl-piperidin-4-ylmethoxy)-quinolin- 4-yloxy]-phenyl}-N′-[2-(4-fluoro-phenyl)-ethyl]-oxalamide 257 N-{3-Fluoro-4-[6-methoxy-7-(1-methyl-piperidin-4-ylmethoxy)-quinolin- 4-yloxy]-phenyl}-N′-phenyl-oxalamide 258 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(3-fluoro-phenyl)-oxalamide 259 N-(4-Chloro-3-fluoro-phenyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 260 N-(3,4-Dimethoxy-phenyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 261 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(3-methyl-butyl)-oxalamide 262 N-(3,3-Dimethyl-butyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 263 N-{5-Chloro-6-[6-methoxy-7-(3-piperidin-1-yl-propoxy)-quinolin-4- yloxy]-pyridin-3-yl}-N′-(4-fluoro-phenyl)-malonamide 264 N-{5-Chloro-6-[6-methoxy-7-(3-morpholin-4-yl-propoxy)-quinolin-4- yloxy]-pyridin-3-yl}-N′-(4-fluoro-phenyl)-malonamide 265 N-{5-Chloro-6-[7-(3-diethylamino-propoxy)-6-methoxy-quinolin-4- yloxy]-pyridin-3-yl}-N′-(4-fluoro-phenyl)-malonamide 266 N-(4-Chloro-benzyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 267 N-(3,5-Dimethoxy-benzyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 268 N-(4-Butyl-benzyl)-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)- quinolin-4-yloxy]-phenyl}-oxalamide 269 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-p-tolyl-ethyl)-oxalamide 270 N-(3,5-Bis-trifluoromethyl-benzyl)-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 271 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-pyrazin-2-ylmethyl-oxalamide 272 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-pyridin-2-ylmethyl-oxalamide 273 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinazolin-4- yloxy]-phenyl}-N′-phenethyl-oxalamide 274 N-{3-Fluoro-4-[6-methoxy-7-(1-methyl-piperidin-4-ylmethoxy)- quinazolin-4-yloxy]-phenyl}-N′-phenethyl-oxalamide 275 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-fluoro-3-trifluoromethyl-benzyl)-oxalamide 276 N-[2-(2-Bromo-6-methoxy-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 277 N-[2-(3,4-Dimethoxy-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-N-methyl-oxalamide 278 N-[2-(5-Bromo-2-methoxy-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 279 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-fluoro-5-trifluoromethyl-benzyl)-oxalamide 280 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-[1-(4-fluoro-phenyl)-ethyl]-oxalamide 281 N-(1S-Benzyl-2-oxo-2-pyrrolidin-1-yl-ethyl)-N′-{3-fluoro-4-[6-methoxy-7- (piperidin-4-ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 282 N-{3-Fluoro-4-[6-methoxy-7-(octahydro-cyclopenta[c]pyrrol-5- ylmethoxy)-quinazolin-4-yloxy]-phenyl}-N′-phenethyl-oxalamide 283 N-[2-(4-Amino-phenyl)-ethyl]-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 284 2-(4-Benzyl-piperidin-1-yl)-N-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-2-oxo-acetamide 285 N-[4-(6,7-Dimethoxy-quinolin-4-yloxy)-phenyl]-N′-(4-fluoro-phenyl)- malonamide 286 N-[5-Chloro-6-(6,7-dimethoxy-quinolin-4-yloxy)-pyridin-3-yl]-N′-(3- fluoro-phenyl)-malonamide 287 N-[5-Chloro-6-(6,7-dimethoxy-quinolin-4-yloxy)-pyridin-3-yl]-N′-phenyl- malonamide 288 N-[5-Chloro-6-(6,7-dimethoxy-quinolin-4-yloxy)-pyridin-3-yl]-N′-(4- fluoro-phenyl)-2,2-dimethyl-malonamide 289 N-Ethyl-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4- yloxy]-phenyl}-oxalamide 290 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-isopropyl-oxalamide 291 N-Butyl-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4- yloxy]-phenyl}-oxalamide 292 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-methoxy-ethyl)-oxalamide 293 N-Cyclopropylmethyl-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4- ylmethoxy)-quinolin-4-yloxy]-phenyl}-oxalamide 294 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-N′-(2-morpholin-4-yl-ethyl)-oxalamide 295 N-{3-Fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4-yloxy]- phenyl}-2-oxo-2-pyrrolidin-1-yl-acetamide 296 N-Ethyl-N′-{3-fluoro-4-[6-methoxy-7-(piperidin-4-ylmethoxy)-quinolin-4- yloxy]-phenyl}-N-methyl-oxalamide

Table 3c Additional Representative c-MET, c-KIT, and/or Flt-3 Inhibitors

The Compounds in Table 3c can be prepared as pharmaceutically acceptable salts, solvates, hydrates, and/or isomers thereof. All such salt, solvate, hydrate, and isomer combinations of the Compounds in Table 3c can be used to practice the invention.

Entry Name 1 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3-yl)-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 2 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3-yl)-N′-(4- fluorophenyl)cyclobutane-1,1-dicarboxamide 3 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3-yl)-N′- (phenylmethyl)cyclopropane-1,1-dicarboxamide 4 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3-yl)-N′- phenylcyclopropane-1,1-dicarboxamide 5 N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4-ylpropyl)oxy]quinolin-4- yl}oxy)phenyl]-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 6 N-[3-fluoro-4-({6-(methyloxy)-7-[(3-piperidin-1-ylpropyl)oxy]quinolin-4- yl}oxy)phenyl]-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 7 N-[3-fluoro-4-({6-(methyloxy)-7-[(3-piperidin-1-ylpropyl)oxy]quinolin-4- yl}oxy)phenyl]-N′-(4-fluorophenyl)cyclobutane-1,1-dicarboxamide 8 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloropyridin-3-yl)-N′-(2- phenylethyl)cyclopropane-1,1-dicarboxamide 9 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-2-methylpyridin-3-yl)-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 10 N-{4-[(7-chloroquinolin-4-yl)oxy]-3-fluorophenyl}-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 11 N-{4-[(7-chloroquinolin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)cyclopropane- 1,1-dicarboxamide 12 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 13 N-(4-{[6,7-bis(methyloxy)quinazolin-4-yl]oxy}phenyl)-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 14 N-(4-{[6,7-bis(methyloxy)quinazolin-4-yl]oxy}-3-fluorophenyl)-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 15 N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4-ylpropyl)oxy]quinazolin-4- yl}oxy)phenyl]-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 16 N-{5-chloro-6-[(6-(methyloxy)-7-{[(1-methylpiperidin-4- yl)methyl]oxy}quinolin-4-yl)oxy]pyridin-3-yl}-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 17 N-[5-chloro-6-({6-(methyloxy)-7-[(piperidin-4-ylmethyl)oxy]quinolin-4- yl}oxy)pyridin-3-yl]-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 18 N-[5-chloro-6-({6-(methyloxy)-7-[(phenylmethyl)oxy]quinolin-4- yl}oxy)pyridin-3-yl]-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 19 N-(4-{[7-{[2-(diethylamino)ethyl]oxy}-6-(methyloxy)quinolin-4-yl]oxy}-3- fluorophenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 20 N-(4-{[7-{[2-(diethylamino)ethyl]oxy}-6-(methyloxy)quinolin-4-yl]oxy}-3- fluorophenyl)-N′-(4-fluorophenyl)cyclobutane-1,1-dicarboxamide 21 N-{3-fluoro-4-[(6-(methyloxy)-7-{[(1-methylpiperidin-4- yl)methyl]oxy}quinazolin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)cyclopropane- 1,1-dicarboxamide 22 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-2-methylphenyl)-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 23 N-(4-fluorophenyl)-N′-[2-methyl-6-({6-(methyloxy)-7-[(3-morpholin-4- ylpropyl)oxy]quinolin-4-yl}oxy)pyridin-3-yl]cyclopropane-1,1-dicarboxamide 24 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 25 N-(6-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-chloro-2-methylpyridin-3-yl)- N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 26 N-[3-fluoro-4-({7-(methyloxy)-6-[(3-morpholin-4-ylpropyl)oxy]quinazolin-4- yl}oxy)phenyl]-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 27 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-3,5-difluorophenyl)-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 28 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-2,5-difluorophenyl)-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 29 N-[3-fluoro-4-({7-(methyloxy)-6-[(3-morpholin-4-ylpropyl)oxy]quinolin-4- yl}oxy)phenyl]-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 30 N-{3-fluoro-4-[(6-(methyloxy)-7-(2-methyl octahydrocyclo-penta[c]pyrrol-5- ylmethoxy)quinazolin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)cyclopropane-1,1- dicarboxamide 31 N-{3-fluoro-4-[(7-(methyloxy)-6-{[(1-methylpiperidin-4- yl)methyl]oxy}quinazolin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)cyclopropane- 1,1-dicarboxamide 32 N-[5-fluoro-2-methyl-4-({6-(methyloxy)-7-[(3-morpholin-4- ylpropyl)oxy]quinolin-4-yl}oxy)phenyl]-N′-(4-fluorophenyl)cyclopropane-1,1- dicarboxamide 33 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-2,3,5-trifluorophenyl)-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 34 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-5-fluoro-2-methylphenyl)-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 35 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-2-chloro-5-methylphenyl)-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 36 N-(3-fluoro-4-{[6-hydroxy-7-(methyloxy)quinolin-4-yl]oxy}phenyl)-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 37 N-(4-fluorophenyl)-N′-[2-methyl-4-({6-(methyloxy)-7-[(3-morpholin-4- ylpropyl)oxy]quinolin-4-yl}oxy)phenyl]cyclopropane-1,1-dicarboxamide 38 N-[3-fluoro-4-({6-(methyloxy)-7-[(3-piperazin-1-ylpropyl)oxy]quinolin-4- yl}oxy)phenyl]-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 39 N-{3-fluoro-4-[(6-(methyloxy)-7-{[3-(4-methylpiperazin-1- yl)propyl]oxy}quinolin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)cyclopropane- 1,1-dicarboxamide 40 N-{3-fluoro-4-[(6-(methyloxy)-7-{[(1-methylpiperidin-4- yl)methyl]oxy}quinolin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)cyclopropane- 1,1-dicarboxamide 41 N-(4-fluorophenyl)-N′-[4-({6-(methyloxy)-7-[(3-morpholin-4- ylpropyl)oxy]quinolin-4-yl}oxy)phenyl]cyclopropane-1,1-dicarboxamide 42 N-(4-{[7-{[3-(diethylamino)propyl]oxy}-6-(methyloxy)quinolin-4-yl]oxy}-3- fluorophenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 43 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}-2-chloro-5-fluorophenyl)-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 44 N-(4-{[6,7-bis(methyloxy)-2-(methylthio)quinolin-4-yl]oxy}-3-fluorophenyl)- N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 45 N-(4-fluorophenyl)-N′-(4-{[2-methyl-6,7-bis(methyloxy)quinazolin-4- yl]oxy}phenyl)cyclopropane-1,1-dicarboxamide 46 N-(4-{[2-amino-6,7-bis(methyloxy)quinolin-4-yl]oxy}-3-fluorophenyl)-N′-(4- fluorophenyl)cyclopropane-1,1-dicarboxamide 47 N-(3-fluoro-4-{[2-(methylamino)-6,7-bis(methyloxy)quinolin-4- yl]oxy}phenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 48 (1S,2R)-N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4- ylpropyl)oxy]quinolin-4-yl}oxy)phenyl]-N′-(4-fluorophenyl)-2- methylcyclopropane-1,1-dicarboxamide 49 (1R,2R)-N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4- ylpropyl)oxy]quinolin-4-yl}oxy)phenyl]-N′-(4-fluorophenyl)-2- methylcyclopropane-1,1-dicarboxamide 50 N-(4-{[6-{[3-(diethylamino)propyl]oxy}-7-(methyloxy)quinolin-4-yl]oxy}-3- fluorophenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 51 N-(4-{[6-{[2-(diethylamino)ethyl]oxy}-7-(methyloxy)quinolin-4-yl]oxy}-3- fluorophenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 52 1,1-dimethylethyl 4-(3-{[4-[(2-fluoro-4-{[(1-{[(4- fluorophenyl)amino]carbonyl}cyclopropyl)carbonyl]amino}phenyl)oxy]-6- (methyloxy)quinolin-7-yl]oxy}propyl)piperazine-1-carboxylate 53 (1R,2R)-N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4- ylpropyl)oxy]quinazolin-4-yl}oxy)phenyl]-N′-(4-fluorophenyl)-2- methylcyclopropane-1,1-dicarboxamide 54 (1R,2R)-N-(4-{[7-{[2-(diethylamino)ethyl]oxy}-6-(methyloxy)quinazolin-4- yl]oxy}-3-fluorophenyl)-N′-(4-fluorophenyl)-2-methylcyclopropane-1,1- dicarboxamide 55 N-(4-{[7-{[3-(diethylamino)propyl]oxy}-6-(methyloxy)quinazolin-4-yl]oxy}-3- fluorophenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 56 N-(4-{[7-{[3-(4-acetylpiperazin-1-yl)propyl]oxy}-6-(methyloxy)quinolin-4- yl]oxy}-3-fluorophenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 57 1,1-dimethylethyl 4-(3-{[4-[(2-fluoro-4-{[((1R,2R)-1-{[(4- fluorophenyl)amino]carbonyl}-2- methylcyclopropyl)carbonyl]amino}phenyl)oxy]-6-(methyloxy)quinolin-7- yl]oxy}propyl)piperazine-1-carboxylate 58 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N′-(4-fluorophenyl)-1- (phenylmethyl)azetidine-3,3-dicarboxamide 59 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N′-(4- fluorophenyl)azetidine-3,3-dicarboxamide 60 (1R,2S)-N-{3-fluoro-4-[(6-(methyloxy)-7-{[3-(4-methylpiperazin-1- yl)propyl]oxy}quinolin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)-2- methylcyclopropane-1,1-dicarboxamide 61 (1R,2R)-N-{3-fluoro-4-[(6-(methyloxy)-7-{[3-(4-methylpiperazin-1- yl)propyl]oxy}quinolin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)-2- methylcyclopropane-1,1-dicarboxamide 62 (1R,2R)-N-[3-fluoro-4-({6-(methyloxy)-7-[(3-piperazin-1- ylpropyl)oxy]quinolin-4-yl}oxy)phenyl]-N′-(4-fluorophenyl)-2- methylcyclopropane-1,1-dicarboxamide 63 N-(3-fluoro-4-{[7-({3-[4-(1-methylethyl)piperazin-1-yl]propyl}oxy)-6- (methyloxy)quinolin-4-yl]oxy}phenyl)-N′-(4-fluorophenyl)cyclopropane-1,1- dicarboxamide 64 N-(4-{[7-{[3-(diethylamino)propyl]oxy}-6-(methyloxy)quinazolin-4-yl]oxy}-3- fluorophenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide 65 (1R,2R)-N-(4-{[7-{[3-(diethylamino)propyl]oxy}-6-(methyloxy)quinolin-4- yl]oxy}-3-fluorophenyl)-N′-(4-fluorophenyl)-2-methylcyclopropane-1,1- dicarboxamide 66 (1R,2R)-N-(4-{[7-{[2-(diethylamino)ethyl]oxy}-6-(methyloxy)quinolin-4- yl]oxy}-3-fluorophenyl)-N′-(4-fluorophenyl)-2-methylcyclopropane-1,1- dicarboxamide 67 (1R,2S)-N-(4-{[7-{[3-(diethylamino)propyl]oxy}-6-(methyloxy)quinolin-4- yl]oxy}-3-fluorophenyl)-N′-(4-fluorophenyl)-2-methylcyclopropane-1,1- dicarboxamide 68 (1R,2S)-N-(4-{[7-{[2-(diethylamino)ethyl]oxy}-6-(methyloxy)quinolin-4- yl]oxy}-3-fluorophenyl)-N′-(4-fluorophenyl)-2-methylcyclopropane-1,1- dicarboxamide 69 N-(4-{[7-{[2-(diethylamino)ethyl]oxy}-6-(methyloxy)quinazolin-4-yl]oxy}-3- fluorophenyl)-N′-(4-fluorophenyl)cyclobutane-1,1-dicarboxamide 70 (1R,2S)-N-[3-fluoro-4-({6-(methyloxy)-7-[(3-piperazin-1- ylpropyl)oxy]quinolin-4-yl}oxy)phenyl]-N′-(4-fluorophenyl)-2- methylcyclopropane-1,1-dicarboxamide 71 (1R,2R,3S)-N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4- ylpropyl)oxy]quinolin-4-yl}oxy)phenyl]-N′-(4-fluorophenyl)-2,3- dimethylcyclopropane-1,1-dicarboxamide 72 (1R,2R,3S)-N-{3-fluoro-4-[(6-(methyloxy)-7-{[3-(4-methylpiperazin-1- yl)propyl]oxy}quinolin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)-2,3- dimethylcyclopropane-1,1-dicarboxamide 73 (1R,2R,3S)-N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4- ylpropyl)oxy]quinazolin-4-yl}oxy)phenyl]-N′-(4-fluorophenyl)-2,3- dimethylcyclopropane-1,1-dicarboxamide 74 (1R,2R,3S)-N-{3-fluoro-4-[(6-(methyloxy)-7-{[3-(4-methylpiperazin-1- yl)propyl]oxy}quinazolin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)-2,3- dimethylcyclopropane-1,1-dicarboxamide 75 N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4-ylpropyl)oxy]quinazolin-4- yl}oxy)phenyl]-N′-(4-fluorophenyl)cyclobutane-1,1-dicarboxamide 76 (2R,3R)-N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4- ylpropyl)oxy]quinolin-4-yl}oxy)phenyl]-N′-(4-fluorophenyl)-2,3- dimethylcyclopropane-1,1-dicarboxamide 77 (2R,3R)-N-(4-{[7-{[3-(diethylamino)propyl]oxy}-6-(methyloxy)quinolin-4- yl]oxy}-3-fluorophenyl)-N′-(4-fluorophenyl)-2,3-dimethylcyclopropane-1,1- dicarboxamide 78 N-(4-{[7-{[3-(diethylamino)propyl]oxy}-6-(methyloxy)quinolin-4-yl]oxy}-3- fluorophenyl)-N′-(4-fluorophenyl)-2,2-dimethylcyclopropane-1,1- dicarboxamide 79 N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4-ylpropyl)oxy]quinazolin-4- yl}oxy)phenyl]-N′-(4-fluorophenyl)-2,2-dimethylcyclopropane-1,1- dicarboxamide 80 (1R,2R,3S)-N-(4-{[7-{[3-(diethylamino)propyl]oxy}-6-(methyloxy)quinolin-4- yl]oxy}-3-fluorophenyl)-N′-(4-fluorophenyl)-2,3-dimethylcyclopropane-1,1- dicarboxamide 81 N-(4-{[7-{[2-(diethylamino)ethyl]oxy}-6-(methyloxy)quinolin-4-yl]oxy}-3- fluorophenyl)-N′-(4-fluorophenyl)-2,2-dimethylcyclopropane-1,1- dicarboxamide 82 (1R,2R,3S)-N-(4-{[7-{[2-(diethylamino)ethyl]oxy}-6-(methyloxy)quinolin-4- yl]oxy}-3-fluorophenyl)-N′-(4-fluorophenyl)-2,3-dimethylcyclopropane-1,1- dicarboxamide 83 N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4-ylpropyl)oxy]quinolin-4- yl}oxy)phenyl]-N′-(4-fluorophenyl)-2,2-dimethylcyclopropane-1,1- dicarboxamide 84 N-(4-{[7-{[2-(diethylamino)ethyl]oxy}-6-(methyloxy)quinazolin-4-yl]oxy}-3- fluorophenyl)-N′-(4-fluorophenyl)-2,2-dimethylcyclopropane-1,1- dicarboxamide 85 N-(4-{[7-{[3-(diethylamino)propyl]oxy}-6-(methyloxy)quinazolin-4-yl]oxy}-3- fluorophenyl)-N′-(4-fluorophenyl)-2,2-dimethylcyclopropane-1,1- dicarboxamide 86 N-(4-{[7-{[3-(diethylamino)propyl]oxy}-6-(methyloxy)quinazolin-4-yl]oxy}-3- fluorophenyl)-N′-(4-fluorophenyl)cyclobutane-1,1-dicarboxamide 87 N-{3-fluoro-4-[(6-(methyloxy)-7-{[3-(4-methylpiperazin-1- yl)propyl]oxy}quinazolin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)cyclobutane- 1,1-dicarboxamide 88 N-[3-fluoro-4-({6-(methyloxy)-7-[(3-piperazin-1-ylpropyl)oxy]quinazolin-4- yl}oxy)phenyl]-N′-(4-fluorophenyl)cyclobutane-1,1-dicarboxamide 89 (2R,3R)-N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4- ylpropyl)oxy]quinazolin-4-yl}oxy)phenyl]-N′-(4-fluorophenyl)-2,3- dimethylcyclopropane-1,1-dicarboxamide 90 N-(4-{[7-{[3-(diethylamino)propyl]oxy}-6-(methyloxy)quinolin-4-yl]oxy}-3- fluorophenyl)-N′-(4-fluorophenyl)cyclobutane-1,1-dicarboxamide 91 N-{3-fluoro-4-[(6-(methyloxy)-7-{[3-(4-methylpiperazin-1- yl)propyl]oxy}quinolin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)cyclobutane-1,1- dicarboxamide 92 (1R,2R)-N-(4-{[7-{[3-(diethylamino)propyl]oxy}-6-(methyloxy)quinazolin-4- yl]oxy}-3-fluorophenyl)-N′-(4-fluorophenyl)-2-methylcyclopropane-1,1- dicarboxamide 93 (1R,2R)-N-{3-fluoro-4-[(6-(methyloxy)-7-{[3-(4-methylpiperazin-1- yl)propyl]oxy}quinazolin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)-2- methylcyclopropane-1,1-dicarboxamide 94 (2R,3R)-N-(4-{[7-{[2-(diethylamino)ethyl]oxy}-6-(methyloxy)quinazolin-4- yl]oxy}-3-fluorophenyl)-N′-(4-fluorophenyl)-2,3-dimethylcyclopropane-1,1- dicarboxamide 95 (2R,3R)-N-(4-{[7-{[3-(diethylamino)propyl]oxy}-6-(methyloxy)quinazolin-4- yl]oxy}-3-fluorophenyl)-N′-(4-fluorophenyl)-2,3-dimethylcyclopropane-1,1- dicarboxamide 96 (1R,2R)-N-[3-fluoro-4-({6-(methyloxy)-7-[(3-piperazin-1- ylpropyl)oxy]quinazolin-4-yl}oxy)phenyl]-N′-(4-fluorophenyl)-2- methylcyclopropane-1,1-dicarboxamide 97 (2R,3R)-N-(4-{[7-{[2-(diethylamino)ethyl]oxy}-6-(methyloxy)quinolin-4- yl]oxy}-3-fluorophenyl)-N′-(4-fluorophenyl)-2,3-dimethylcyclopropane-1,1- dicarboxamide 98 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N′-[(4- fluorophenyl)methyl]cyclopropane-1,1-dicarboxamide 99 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N′-(2-morpholin-4- ylethyl)cyclopropane-1,1-dicarboxamide 100 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N′-[2-(piperidin-1- ylmethyl)phenyl]cyclopropane-1,1-dicarboxamide 101 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N′-[2-(pyrrolidin-1- ylmethyl)phenyl]cyclopropane-1,1-dicarboxamide 102 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N′-[3-(morpholin-4- ylmethyl)phenyl]cyclopropane-1,1-dicarboxamide 103 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N′-[2-(morpholin-4- ylmethyl)phenyl]cyclopropane-1,1-dicarboxamide 104 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N′-phenylcyclopropane- 1,1-dicarboxamide 105 N-[3-(aminomethyl)phenyl]-N′-(4-{[6,7-bis(methyloxy)quinolin-4- yl]oxy}phenyl)cyclopropane-1,1-dicarboxamide 106 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N′-[3-(piperidin-1- ylmethyl)phenyl]cyclopropane-1,1-dicarboxamide 107 N-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-N′-[3-(pyrrolidin-1- ylmethyl)phenyl]cyclopropane-1,1-dicarboxamide

Table 4 Representative EGFR, ErbB2, and/or VEGFR Inhibitors

The Compounds in Table 4 can be prepared as pharmaceutically acceptable salts, solvates, hydrates, and/or isomers thereof. All such salt, solvate, hydrate, and isomer combinations of the Compounds in Table 4 can be used to practice the invention. In particular, the invention can be practiced with one or two pharmaceutically acceptable salts of a Compound of Table 4 which salt(s) are formed with one or two acids independently selected from hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, acetic acid, trifluoroacetic acid, propionic acid, hexanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, 3-(4-hydroxybenzoyl)benzoic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, 1,2-ethanedisulfonic acid, 2-hydroxyethanesulfonic acid, benzenesulfonic acid, 4-chlorobenzenesulfonic acid, 2-naphthalenesulfonic acid, 4-toluenesulfonic acid, camphorsulfonic acid, glucoheptonic acid, 4,4′-methylenebis-(3-hydroxy-2-ene-1-carboxylic acid), 3-phenylpropionic acid, trimethylacetic acid, tertiary butylacetic acid, lauryl sulfuric acid, gluconic acid, glutamic acid, hydroxynaphthoic acid, salicylic acid, stearic acid, muconic acid, p-toluenesulfonic acid, and salicylic acid.

Entry Name 1 N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-(1- methylethyl)octahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6- (methyloxy)quinazolin-4-amine 2 N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-(1- methylethyl)octahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6- (methyloxy)quinazolin-4-amine 3 7-({[(3aR,5r,6aS)-2-acetyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-N-(4- bromo-3-chloro-2-fluorophenyl)-6-(methyloxy)quinazolin-4-amine 4 N-(4-bromo-3-chloro-2-fluorophenyl)-6-(methyloxy)-7-{[(3aR,5r,6aS)- octahydrocyclopenta[c]pyrrol-5-ylmethyl]oxy}quinazolin-4-amine 5 ethyl (3aR,6aS)-5-({[4-[(4-bromo-3-chloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]oxy}methyl)hexahydrocyclopenta[c]pyrrole-2(1H)- carboxylate 6 N-(4-bromo-3-chloro-2-fluorophenyl)-6-(methyloxy)-7-({[(3aR,5r,6aS)-2- (methylsulfonyl)octahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)quinazolin-4- amine 7 N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2- ethyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4- amine 8 N-(3,4-dichloro-2-fluorophenyl)-6-(methyloxy)-7-({[(3aR,5r,6aS)-2-(2- methylpropyl)octahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)quinazolin-4-amine 9 N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2- methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin- 4-amine 10 N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2- methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin- 4-amine 11 N-(3-chloro-2,4-difluorophenyl)-7-({[(3aR,5s,6aS)-2- methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin- 4-amine 12 N-(4,5-dichloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2- methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin- 4-amine 13 N-(4-bromo-5-chloro-2-fluorophenyl)-7-({[(3aR,5s,6aS)-2- methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin- 4-amine 14 N-(4-bromo-2,3-dichlorophenyl)-7-({[(3aR,5s,6aS)-2- methyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin- 4-amine 15 N-(3,4-dichlorophenyl)-7-({[(3aR,5s,6aS)-2-methyloctahydrocyclopenta[c]pyrrol- 5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 16 N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2- ethyloctahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4- amine 17 N-(4-bromo-3-chloro-2-fluorophenyl)-6-(methyloxy)-7-({[(3aR,5r,6aS)-2-(2- methylpropyl)octahydrocyclopenta[c]pyrrol-5-yl]methyl}oxy)quinazolin-4-amine 18 N-(4-bromo-2,3-dichlorophenyl)-7-{[(3R,9aS)-hexahydro-1H-[1,4]oxazino[3,4- c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 19 N-(4,5-dichloro-2-fluorophenyl)-7-{[(3R,9aS)-hexahydro-1H-[1,4]oxazino[3,4- c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 20 N-(4-bromo-5-chloro-2-fluorophenyl)-7-{[(3R,9aS)-hexahydro-1H- [1,4]oxazino[3,4-c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 21 N-(3-chloro-2,4-difluorophenyl)-7-{[(3R,9aS)-hexahydro-1H-[1,4]oxazino[3,4- c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 22 N-(3,4-dichloro-2-fluorophenyl)-7-{[(3S,9aS)-hexahydro-1H-[1,4]oxazino[3,4- c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 23 N-(4-bromo-3-chloro-2-fluorophenyl)-7-{[(3S,9aS)-hexahydro-1H- [1,4]oxazino[3,4-c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 24 N-(3-chloro-2,4-difluorophenyl)-7-{[(3S,9aS)-hexahydro-1H-[1,4]oxazino[3,4- c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 25 N-(3,4-dichlorophenyl)-7-[(hexahydro-1H-[1,4]oxazino[3,4-c][1,4]oxazin-3- ylmethyl)oxy]-6-(methyloxy)quinazolin-4-amine 26 N-(4,5-dichloro-2-fluorophenyl)-7-{[(3S,9aS)-hexahydro-1H-[1,4]oxazino[3,4- c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 27 N-(4-bromo-2,3-dichlorophenyl)-7-{[(3S,9aS)-hexahydro-1H-[1,4]oxazino[3,4- c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 28 N-(4-bromo-5-chloro-2-fluorophenyl)-7-{[(3S,9aS)-hexahydro-1H- [1,4]oxazino[3,4-c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 29 N-(3,4-dichloro-2-fluorophenyl)-7-{[(3R,9aS)-hexahydro-1H-[1,4]oxazino[3,4- c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 30 N-(4-bromo-3-chloro-2-fluorophenyl)-7-{[(3R,9aS)-hexahydro-1H- [1,4]oxazino[3,4-c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 31 N-(3,4-dichlorophenyl)-7-{[(3R,8aR)-hexahydro-1H-pyrrolo[2,1-c][1,4]oxazin-3- ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 32 N-(4-bromo-5-chloro-2-fluorophenyl)-7-{[(3S,8aS)-hexahydro-1H-pyrrolo[2,1- c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 33 N-(3,4-dichlorophenyl)-7-{[(3S,8aR)-hexahydro-1H-pyrrolo[2,1-c][1,4]oxazin-3- ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 34 N-(3,4-dichlorophenyl)-7-{[(3S,8aS)-hexahydro-1H-pyrrolo[2,1-c][1,4]oxazin-3- ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 35 N-(3,4-dichlorophenyl)-7-{[(3R,8aS)-hexahydro-1H-pyrrolo[2,1-c][1,4]oxazin-3- ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 36 N-(3,4-dichloro-2-fluorophenyl)-7-{[(3S,8aS)-hexahydro-1H-pyrrolo[2,1- c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 37 N-(4-bromo-3-chloro-2-fluorophenyl)-7-{[(3S,8aS)-hexahydro-1H-pyrrolo[2,1- c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 38 N-(3-chloro-2,4-difluorophenyl)-7-{[(3S,8aS)-hexahydro-1H-pyrrolo[2,1- c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 39 N-(4-bromo-2,3-dichlorophenyl)-7-{[(3S,8aS)-hexahydro-1H-pyrrolo[2,1- c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 40 N-(4,5-dichloro-2-fluorophenyl)-7-{[(3S,8aS)-hexahydro-1H-pyrrolo[2,1- c][1,4]oxazin-3-ylmethyl]oxy}-6-(methyloxy)quinazolin-4-amine 41 1,4:3,6-dianhydro-5-({[4-[(4-bromo-5-chloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]oxy}methyl)-5-deoxy-2-O-methyl-D-xylo-hexitol 42 1,4:3,6-dianhydro-5-deoxy-5-({[4-[(3,4-dichlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]oxy}methyl)-2-O-methyl-D-glucitol 43 1,4:3,6-dianhydro-5-deoxy-5-({[4-[(3,4-dichloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]oxy}methyl)-2-O-methyl-D-xylo-hexitol 44 1,4:3,6-dianhydro-5-({[4-[(4-bromo-3-chloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]oxy}methyl)-5-deoxy-2-O-methyl-D-xylo-hexitol 45 1,4:3,6-dianhydro-5-({[4-[(3-chloro-2,4-difluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]oxy}methyl)-5-deoxy-2-O-methyl-D-xylo-hexitol 46 1,4:3,6-dianhydro-5-({[4-[(4-bromo-2,3-dichlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]oxy}methyl)-5-deoxy-2-O-methyl-D-glucitol 47 1,4:3,6-dianhydro-2-deoxy-2-({[4-[(3,4-dichlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]oxy}methyl)-5-O-methyl-D-threo-hexitol 48 1,4:3,6-dianhydro-5-deoxy-5-({[4-[(4,5-dichloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]oxy}methyl)-2-O-methyl-D-glucitol 49 (3S,9aS)-3-({[4-[(3,4-dichloro-2-fluorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)hexahydro-2H-pyrido[1,2-a]pyrazin-1(6H)-one 50 (3S,9aR)-3-({[4-[(3,4-dichloro-2-fluorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)hexahydro-2H-pyrido[1,2-a]pyrazin-1(6H)-one 51 (3S,8aS)-3-({[4-[(3,4-dichloro-2-fluorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)hexahydropyrrolo[1,2-a]pyrazin-1(2H)-one 52 (3S,8aR)-3-({[4-[(3,4-dichloro-2-fluorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)hexahydropyrrolo[1,2-a]pyrazin-1(2H)-one 53 (3S,8aS)-3-({[4-[(4-bromo-3-chloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]oxy}methyl)hexahydropyrrolo[1,2-a]pyrazin-1(2H)- one 54 (3S,8aS)-3-({[4-[(3,4-dichloro-2-fluorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)-2-methylhexahydropyrrolo[1,2-a]pyrazin-1(2H)-one 55 N-(3,4-dichlorophenyl)-7-({2-[(8-methyl-8-azabicyclo[3.2.1]oct-3- yl)amino]ethyl}oxy)-6-(methyloxy)quinazolin-4-amine 56 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(8aR)-tetrahydro-1H-[1,3]thiazolo[4,3- c][1,4]oxazin-6-ylmethyl]oxy}quinazolin-4-amine 57 N-(3,4-dichlorophenyl)-7-{[2-(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)ethyl]oxy}-6- (methyloxy)quinazolin-4-amine 58 N-(3,4-dichlorophenyl)-7-{[(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 59 N-(3,4-dichlorophenyl)-7-{[(3aR,6aS)-2-methyloctahydrocyclopenta[c]pyrrol-5- yl]oxy}-6-(methyloxy)quinazolin-4-amine 60 N-(3,4-dichlorophenyl)-7-[(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)oxy]-6- (methyloxy)quinazolin-4-amine 61 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-5-chloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-methyl-L-iditol 62 1,4:3,6-dianhydro-2-O-[4-[(3,4-dichloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-methyl-L-iditol 63 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-methyl-L-iditol 64 1,4:3,6-dianhydro-2-O-methyl-5-O-{6-(methyloxy)-4-[(2,3,4- trichlorophenyl)amino]quinazolin-7-yl}-L-iditol 65 1,4:3,6-dianhydro-5-O-[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin- 7-yl]-2-O-methyl-D-xylo-hexitol 66 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-2,3-dichlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-methyl-L-iditol 67 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6-(methyloxy)- quinazolin-7-yl]-sorbose ethylene glycol acetal 68 1,4:3,6-dianhydro-2-O-[4-[(3-chloro-2,4-difluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-methyl-L-iditol 69 1,4:3,6-dianhydro-2-O-[4-[(4,5-dichloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-methyl-L-iditol 70 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-(difluoromethyl)-L-iditol 71 1,4:3,6-dianhydro-2-O-[4-[(3-chloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-methyl-L-iditol 72 1,4:3,6-dianhydro-2-O-[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin- 7-yl]-5-O-methyl-L-iditol 73 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-methyl-L-iditol 74 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-ethyl-L-iditol 75 1,4:3,6-dianhydro-2-O-[4-[(3-bromo-2-methylphenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-methyl-L-iditol 76 1,4:3,6-dianhydro-2-O-[4-[(3-chloro-2-methylphenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-methyl-L-iditol 77 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-deoxy-D-xylo-hexitol 78 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-methyl-D-glucitol 79 methyl 3,6-anhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-O-methyl-alpha-L-idofuranoside 80 3,6-anhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6-(methyloxy)quinazolin- 7-yl]-1,2-O-(1-methylethylidene)-beta-L-xylo-hexofuranose 81 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-deoxy-5-methylidene-D-xylo-hexitol 82 methyl 3,6-anhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-O-methyl-beta-L-idofuranoside 83 N-(3,4-dichloro-2-fluorophenyl)-6-(methyloxy)-7-[(octahydro-2H-quinolizin-3- ylmethyl)oxy]quinazolin-4-amine 84 1,4:3,6-dianhydro-2-deoxy-2-fluoro-5-O-{6-(methyloxy)-4-[(2,3,4- trifluorophenyl)amino]quinazolin-7-yl}-D-iditol 85 1,4:3,6-dianhydro-5-O-[4-[(2-chloro-4-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 86 1,4:3,6-dianhydro-5-O-[4-[(2-bromo-4-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 87 1,4:3,6-dianhydro-2-deoxy-5-O-[4-[(2,6-difluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-fluoro-D-iditol 88 1,4:3,6-dianhydro-5-O-[4-[(3-chloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 89 1,4:3,6-dianhydro-2-deoxy-2-fluoro-5-O-[4-{[4-fluoro-3- (trifluoromethyl)phenyl]amino}-6-(methyloxy)quinazolin-7-yl]-D-iditol 90 1,4:3,6-dianhydro-2-deoxy-5-O-[4-[(2,4-difluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-fluoro-D-iditol 91 1,4:3,6-dianhydro-2-deoxy-5-O-[4-[(2,5-difluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-fluoro-D-iditol 92 1,4:3,6-dianhydro-2-deoxy-5-O-[4-[(2,3-difluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-fluoro-D-iditol 93 1,4:3,6-dianhydro-5-O-[4-[(5-chloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 94 1,4:3,6-dianhydro-2-deoxy-5-O-[4-[(3,5-difluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-fluoro-D-iditol 95 1,4:3,6-dianhydro-5-O-[4-[(3-chloro-4-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 96 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-2-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 97 1,4:3,6-dianhydro-2-deoxy-5-O-[4-[(3,4-dichloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-fluoro-D-iditol 98 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-5-chloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 99 1,4:3,6-dianhydro-2-deoxy-2-fluoro-5-O-{6-(methyloxy)-4-[(2,4,5- trifluorophenyl)amino]quinazolin-7-yl}-D-iditol 100 1,4:3,6-dianhydro-2-deoxy-2-fluoro-5-O-{6-(methyloxy)-4-[(2,4,6- trifluorophenyl)amino]quinazolin-7-yl}-D-iditol 101 1,4:3,6-dianhydro-5-O-[4-({4-[(4-chlorophenyl)oxy]-3,5-difluorophenyl}amino)- 6-(methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 102 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 103 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-2,3-dichlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 104 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chloro-5-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 105 1,4:3,6-dianhydro-2-deoxy-5-O-[4-[(4,5-dichloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-fluoro-D-iditol 106 1,4:3,6-dianhydro-2-deoxy-2-fluoro-5-O-{6-(methyloxy)-4-[(2,3,4- trichlorophenyl)amino]quinazolin-7-yl}-D-iditol 107 1,4:3,6-dianhydro-2-deoxy-2-fluoro-5-O-{6-(methyloxy)-4-[(3,4,5- trichlorophenyl)amino]quinazolin-7-yl}-D-iditol 108 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 109 1,4:3,6-dianhydro-5-O-[4-[(4-chloro-2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 110 1,4:3,6-dianhydro-5-O-[4-[(3-chloro-2-methylphenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 111 1,4:3,6-dianhydro-2-deoxy-5-O-[4-[(3,4-difluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-fluoro-D-iditol 112 1,4:3,6-dianhydro-5-O-[4-[(2-chlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]-2-deoxy-2-fluoro-D-iditol 113 1,4:3,6-dianhydro-2-deoxy-2-fluoro-5-O-[4-[(2-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-D-iditol 114 1,4:3,6-dianhydro-5-O-[4-[(3-chlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]-2-deoxy-2-fluoro-D-iditol 115 1,4:3,6-dianhydro-2-deoxy-2-fluoro-5-O-[4-[(4-fluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-D-iditol 116 1,4:3,6-dianhydro-5-O-[4-[(4-chlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]-2-deoxy-2-fluoro-D-iditol 117 1,4:3,6-dianhydro-2-deoxy-5-O-[4-[(2,4-dichlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-fluoro-D-iditol 118 1,4:3,6-dianhydro-2-deoxy-5-O-[4-[(2,5-dichlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-fluoro-D-iditol 119 1,4:3,6-dianhydro-2-deoxy-5-O-[4-[(3,4-dichlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-fluoro-D-iditol 120 1,4:3,6-dianhydro-5-O-[4-[(2-bromo-4,6-difluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 121 1,4:3,6-dianhydro-5-O-[4-{[4-chloro-3-(trifluoromethyl)phenyl]amino}-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 122 1,4:3,6-dianhydro-5-O-[4-{[2-chloro-5-(trifluoromethyl)phenyl]amino}-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 123 1,4:3,6-dianhydro-2-deoxy-2-fluoro-5-O-[4-{[2-fluoro-3- (trifluoromethyl)phenyl]amino}-6-(methyloxy)quinazolin-7-yl]-D-iditol 124 1,4:3,6-dianhydro-5-O-[4-{[2-bromo-5-(trifluoromethyl)phenyl]amino}-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 125 1,4:3,6-dianhydro-5-O-[4-{[2-bromo-4-(trifluoromethyl)phenyl]amino}-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 126 1,4:3,6-dianhydro-2-deoxy-2-fluoro-5-O-[4-{[4-fluoro-2- (trifluoromethyl)phenyl]amino}-6-(methyloxy)quinazolin-7-yl]-D-iditol 127 1,4:3,6-dianhydro-5-O-[4-{[3-bromo-5-(trifluoromethyl)phenyl]amino}-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 128 1,4:3,6-dianhydro-5-O-[4-[(2-bromophenyl)amino]-6-(methyloxy)quinazolin-7- yl]-2-deoxy-2-fluoro-D-iditol 129 1,4:3,6-dianhydro-5-O-[4-[(3-bromophenyl)amino]-6-(methyloxy)quinazolin-7- yl]-2-deoxy-2-fluoro-D-iditol 130 1,4:3,6-dianhydro-5-O-[4-[(4-bromophenyl)amino]-6-(methyloxy)quinazolin-7- yl]-2-deoxy-2-fluoro-D-iditol 131 1,4:3,6-dianhydro-5-O-[4-[(3-bromo-4-methylphenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 132 1,4:3,6-dianhydro-5-O-[4-[(5-chloro-2-methylphenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 133 1,4:3,6-dianhydro-2-deoxy-5-O-[4-[(3,5-dimethylphenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-fluoro-D-iditol 134 1,4:3,6-dianhydro-5-O-[4-{[2,5-bis(methyloxy)phenyl]amino}-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 135 1,4:3,6-dianhydro-5-O-[4-{[5-chloro-2,4-bis(methyloxy)phenyl]amino}-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 136 1,4:3,6-dianhydro-5-O-[4-{[4-chloro-2,5-bis(methyloxy)phenyl]amino}-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 137 1,4:3,6-dianhydro-5-O-[4-[(3-chloro-2,4-difluorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-fluoro-D-iditol 138 N-(3,4-dichlorophenyl)-7-[({5-[(dimethylamino)methyl]-1,2,4-oxadiazol-3- yl}methyl)oxy]-6-(methyloxy)quinazolin-4-amine 139 N-(3,4-dichlorophenyl)-7-[({3-[(dimethylamino)methyl]-1,2,4-oxadiazol-5- yl}methyl)oxy]-6-(methyloxy)quinazolin-4-amine 140 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({3-[(4-methylpiperazin-1-yl)methyl]- 1,2,4-oxadiazol-5-yl}methyl)oxy]quinazolin-4-amine 141 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(5-piperidin-4-yl-1,2,4-oxadiazol-3- yl)methyl]oxy}quinazolin-4-amine 142 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[5-(1-methylpiperidin-4-yl)-1,2,4- oxadiazol-3-yl]methyl}oxy)quinazolin-4-amine 143 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[3-(morpholin-4-ylmethyl)-1,2,4- oxadiazol-5-yl]methyl}oxy)quinazolin-4-amine 144 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[(morpholin-2-ylmethyl)oxy]quinazolin- 4-amine 145 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(5-piperidin-2-yl-1,2,4-oxadiazol-3- yl)methyl]oxy}quinazolin-4-amine 146 N-(3,4-dichlorophenyl)-7-[({2-[(dimethylamino)methyl]-1,3-thiazol-4- yl}methyl)oxy]-6-(methyloxy)quinazolin-4-amine 147 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(phenylmethyl)morpholin-2- yl]methyl}oxy)quinazolin-4-amine 148 1,1-dimethylethyl 2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholine-4-carboxylate 149 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[2-(morpholin-4-ylmethyl)-1,3-thiazol- 4-yl]methyl}oxy)quinazolin-4-amine 150 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({2-[(4-methylpiperazin-1-yl)methyl]- 1,3-thiazol-4-yl}methyl)oxy]quinazolin-4-amine 151 N-(3,4-dichlorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 152 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[(1,4-oxazepan-2- ylmethyl)oxy]quinazolin-4-amine 153 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(5-piperidin-3-yl-1,2,4-oxadiazol-3- yl)methyl]oxy}quinazolin-4-amine 154 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[5-(1-methylpiperidin-2-yl)-1,2,4- oxadiazol-3-yl]methyl}oxy)quinazolin-4-amine 155 N-(3,4-dichlorophenyl)-7-{[(4-methyl-1,4-oxazepan-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 156 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[5-(1-methylpiperidin-3-yl)-1,2,4- oxadiazol-3-yl]methyl}oxy)quinazolin-4-amine 157 N-(3,4-dichlorophenyl)-7-({[5-(1,1-dimethylethyl)-1,2,4-oxadiazol-3- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 158 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(2-phenyl-1,3-thiazol-4- yl)methyl]oxy}quinazolin-4-amine 159 7-[(2,1,3-benzothiadiazol-4-ylmethyl)oxy]-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 160 N-(3,4-dichlorophenyl)-7-{[(5-methylisoxazol-3-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 161 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(5-methyl-4-phenylisoxazol-3- yl)methyl]oxy}quinazolin-4-amine 162 7-[(1,3-benzothiazol-2-ylmethyl)oxy]-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 163 7-[(2,1,3-benzoxadiazol-5-ylmethyl)oxy]-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 164 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[2-(2-thienyl)-1,3-thiazol-4- yl]methyl}oxy)quinazolin-4-amine 165 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(1-phenyl-1H-pyrazol-4- yl)methyl]oxy}quinazolin-4-amine 166 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({5-[3-(trifluoromethyl)phenyl]-1,2,4- oxadiazol-3-yl}methyl)oxy]quinazolin-4-amine 167 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({5-[4-(trifluoromethyl)phenyl]-1,2,4- oxadiazol-3-yl}methyl)oxy]quinazolin-4-amine 168 7-({[3-(4-chlorophenyl)-1,2,4-oxadiazol-5-yl]methyl}oxy)-N-(3,4- dichlorophenyl)-6-(methyloxy)quinazolin-4-amine 169 7-({[6-bromo-2-(methyloxy)naphthalen-1-yl]methyl}oxy)-N-(3,4-dichlorophenyl)- 6-(methyloxy)quinazolin-4-amine 170 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[(1,3-thiazol-4-ylmethyl)oxy]quinazolin- 4-amine 171 7-{[(6-chloropyridin-3-yl)methyl]oxy}-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 172 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[(pyridin-4-ylmethyl)oxy]quinazolin-4- amine 173 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(2-methyl-1,3-thiazol-4- yl)methyl]oxy}quinazolin-4-amine 174 7-{[(6-chloro-4H-1,3-benzodioxin-8-yl)methyl]oxy}-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 175 7-{[(5-chloro-1-methyl-3-phenyl-1H-pyrazol-4-yl)methyl]oxy}-N-(3,4- dichlorophenyl)-6-(methyloxy)quinazolin-4-amine 176 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[1-methyl-3-(trifluoromethyl)-1H- thieno[2,3-c]pyrazol-5-yl]methyl}oxy)quinazolin-4-amine 177 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(3-phenylisoxazol-5- yl)methyl]oxy}quinazolin-4-amine 178 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(2,4,6- trimethylphenyl)methyl]oxy}quinazolin-4-amine 179 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[(pyridin-3-ylmethyl)oxy]quinazolin-4- amine 180 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({3-[4-(methyloxy)phenyl]isoxazol-5- yl}methyl)oxy]quinazolin-4-amine 181 N-(3,4-dichlorophenyl)-7-({[5-[(2,4-dichlorophenyl)oxy]-1-methyl-3- (trifluoromethyl)-1H-pyrazol-4-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 182 7-[(cyclopropylmethyl)oxy]-N-(3,4-dichlorophenyl)-6-(methyloxy)quinazolin-4- amine 183 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[(tetrahydrofuran-2- ylmethyl)oxy]quinazolin-4-amine 184 7-(cyclopentyloxy)-N-(3,4-dichlorophenyl)-6-(methyloxy)quinazolin-4-amine 185 7-[(2-cyclohexylethyl)oxy]-N-(3,4-dichlorophenyl)-6-(methyloxy)quinazolin-4- amine 186 7-[(cyclohexylmethyl)oxy]-N-(3,4-dichlorophenyl)-6-(methyloxy)quinazolin-4- amine 187 7-[(cyclobutylmethyl)oxy]-N-(3,4-dichlorophenyl)-6-(methyloxy)quinazolin-4- amine 188 N-(3,4-dichlorophenyl)-7-{[2-(1,3-dioxolan-2-yl)ethyl]oxy}-6- (methyloxy)quinazolin-4-amine 189 N-(3,4-dichlorophenyl)-7-{[2-(1,3-dioxan-2-yl)ethyl]oxy}-6- (methyloxy)quinazolin-4-amine 190 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[(2-morpholin-4-ylethyl)oxy]quinazolin- 4-amine 191 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[(2-pyrrolidin-1-ylethyl)oxy]quinazolin- 4-amine 192 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[(2-piperidin-1-ylethyl)oxy]quinazolin-4- amine 193 2-(2-{[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7-yl]oxy}ethyl)- 1H-isoindole-1,3(2H)-dione 194 methyl 6-O-[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7-yl]-alpha- D-glucopyranoside 195 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[(2-morpholin-4-yl-2- oxoethyl)oxy]quinazolin-4-amine 196 1,1-dimethylethyl 2-[3-({[4-[(3,4-dichlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]oxy}methyl)-1,2,4-oxadiazol-5-yl]piperidine-1- carboxylate 197 1,1-dimethylethyl 4-[3-({[4-[(3,4-dichlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]oxy}methyl)-1,2,4-oxadiazol-5-yl]piperidine-1- carboxylate 198 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(4-pyrrolidin-1-ylphenyl)-1,3- thiazol-2-yl]methyl}oxy)quinazolin-4-amine 199 N-(3,4-dichlorophenyl)-7-[({4-[4-(diethylamino)phenyl]-1,3-thiazol-2- yl}methyl)oxy]-6-(methyloxy)quinazolin-4-amine 200 5-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)-1,3-thiazol-4-yl]-2-hydroxybenzamide 201 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4-pyridin-3-yl-1,3-thiazol-2- yl)methyl]oxy}quinazolin-4-amine 202 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4-pyridin-2-yl-1,3-thiazol-2- yl)methyl]oxy}quinazolin-4-amine 203 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4-pyridin-4-yl-1,3-thiazol-2- yl)methyl]oxy}quinazolin-4-amine 204 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(2-morpholin-4-yl-1,3-thiazol-4- yl)methyl]oxy}quinazolin-4-amine 205 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(3-morpholin-4-yl-1,2,4-oxadiazol-5- yl)methyl]oxy}quinazolin-4-amine 206 N-(3,4-dichlorophenyl)-7-({[3-(dimethylamino)-1,2,4-oxadiazol-5- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 207 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({4-[(4-methylpiperazin-1-yl)methyl]- 1,3-thiazol-2-yl}methyl)oxy]quinazolin-4-amine 208 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[(4,5,6,7-tetrahydro[1,3]thiazolo[5,4- c]pyridin-2-ylmethyl)oxy]quinazolin-4-amine 209 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(morpholin-4-ylmethyl)-1,3-thiazol- 2-yl]methyl}oxy)quinazolin-4-amine 210 N-(3,4-dichlorophenyl)-7-[({4-[(4-methyl-1,4-diazepan-1-yl)methyl]-1,3-thiazol-2- yl}methyl)oxy]-6-(methyloxy)quinazolin-4-amine 211 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(5-{[(phenylmethyl)oxy]methyl}-1,2,4- oxadiazol-3-yl)methyl]oxy}quinazolin-4-amine 212 N-(3,4-dichlorophenyl)-7-{[(4-ethylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 213 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(2-piperidin-4-yl-1,3-thiazol-4- yl)methyl]oxy}quinazolin-4-amine 214 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[2-(1-methylpiperidin-4-yl)-1,3-thiazol- 4-yl]methyl}oxy)quinazolin-4-amine 215 1,1-dimethylethyl 4-[5-({[4-[(3,4-dichlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]oxy}methyl)-1,2,4-oxadiazol-3-yl]piperazine-1- carboxylate 217 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(3-piperazin-1-yl-1,2,4-oxadiazol-5- yl)methyl]oxy}quinazolin-4-amine 218 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[3-(4-methylpiperazin-1-yl)-1,2,4- oxadiazol-5-yl]methyl}oxy)quinazolin-4-amine 219 N-(3,4-dichlorophenyl)-7-({[5-(1-ethylpiperidin-2-yl)-1,2,4-oxadiazol-3- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 220 N-(3,4-dichlorophenyl)-7-({[3-(4-ethylpiperazin-1-yl)-1,2,4-oxadiazol-5- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 221 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({5-[4-(methyloxy)phenyl]-1,2,4- oxadiazol-3-yl}methyl)oxy]quinazolin-4-amine 222 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({2-[4-(trifluoromethyl)phenyl]-1,3- thiazol-4-yl}methyl)oxy]quinazolin-4-amine 223 7-({[2-(4-chlorophenyl)-1,3-thiazol-4-yl]methyl}oxy)-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 224 N-(3,4-dichlorophenyl)-7-({[5-(3,5-dimethylisoxazol-4-yl)-1,2,4-oxadiazol-3- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 225 7-{[(5-chloro-1-benzothien-3-yl)methyl]oxy}-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 226 N-(3,4-dichlorophenyl)-7-[({3-[4-(1,1-dimethylethyl)phenyl]-1,2,4-oxadiazol-5- yl}methyl)oxy]-6-(methyloxy)quinazolin-4-amine 227 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({5-[2-(methyloxy)phenyl]-1,2,4- oxadiazol-3-yl}methyl)oxy]quinazolin-4-amine 228 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[5-(4-methylphenyl)-1,3,4-oxadiazol-2- yl]methyl}oxy)quinazolin-4-amine 229 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[1-(phenylmethyl)-1H-imidazol-2- yl]methyl}oxy)quinazolin-4-amine 230 N-(3,4-dichlorophenyl)-7-({[3-(2,6-dichlorophenyl)-5-methylisoxazol-4- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 231 N-(3,4-dichlorophenyl)-7-{[(6-fluoro-4H-1,3-benzodioxin-8-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 232 7-{[(3,5-dibromophenyl)methyl]oxy}-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 233 N-(3,4-dichlorophenyl)-7-{[(2,6-difluorophenyl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 234 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({3-[(pyridin-2-ylsulfonyl)methyl]- 1,2,4-oxadiazol-5-yl}methyl)oxy]quinazolin-4-amine 235 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(5-phenyl-1,2,4-oxadiazol-3- yl)methyl]oxy}quinazolin-4-amine 236 7-({[4-chloro-2-(trifluoromethyl)quinolin-6-yl]methyl}oxy)-N-(3,4- dichlorophenyl)-6-(methyloxy)quinazolin-4-amine 237 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[2-(1-methylpyrrolidin-2- yl)ethyl]oxy}quinazolin-4-amine 238 N-(3,4-dichlorophenyl)-7-({[5-(1-ethylpiperidin-4-yl)-1,2,4-oxadiazol-3- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 239 N-(3,4-dichlorophenyl)-7-({[5-(1-ethylpiperidin-3-yl)-1,2,4-oxadiazol-3- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 240 N-(3,4-dichlorophenyl)-7-({[2-(dimethylamino)-1,3-thiazol-4-yl]methyl}oxy)-6- (methyloxy)quinazolin-4-amine 241 N-(3,4-dichlorophenyl)-7-{[(4-ethyl-1,4-oxazepan-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 242 N-(3,4-dichlorophenyl)-7-({[2-(1-ethylpiperidin-4-yl)-1,3-thiazol-4- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 243 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({3-[(2S)-pyrrolidin-2-yl]-1,2,4- oxadiazol-5-yl}methyl)oxy]quinazolin-4-amine 244 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({2-[(2S)-pyrrolidin-2-yl]-1,3-thiazol-4- yl}methyl)oxy]quinazolin-4-amine 245 [4-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7-yl]oxy}methyl)- 1,3-thiazol-2-yl]methyl benzoate 246 [4-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7-yl]oxy}methyl)- 1,3-thiazol-2-yl]methanol 247 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(5-methyl-4,5,6,7- tetrahydro[1,3]thiazolo[5,4-c]pyridin-2-yl)methyl]oxy}quinazolin-4-amine 248 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({2-[(4S)-1,3-thiazolidin-4-yl]-1,3- thiazol-4-yl}methyl)oxy]quinazolin-4-amine 249 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(2-piperidin-2-yl-1,3-thiazol-4- yl)methyl]oxy}quinazolin-4-amine 250 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[2-(1-methylpiperidin-2-yl)-1,3-thiazol- 4-yl]methyl}oxy)quinazolin-4-amine 251 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(2-piperidin-3-yl-1,3-thiazol-4- yl)methyl]oxy}quinazolin-4-amine 252 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[2-(1-methylpiperidin-3-yl)-1,3-thiazol- 4-yl]methyl}oxy)quinazolin-4-amine 253 N-(3,4-dichlorophenyl)-7-({[2-(1-ethylpiperidin-2-yl)-1,3-thiazol-4- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 254 N-(3,4-dichlorophenyl)-7-({[2-(1-ethylpiperidin-3-yl)-1,3-thiazol-4- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 255 N-(3,4-dichlorophenyl)-7-[({3-[(2S)-1-ethylpyrrolidin-2-yl]-1,2,4-oxadiazol-5- yl}methyl)oxy]-6-(methyloxy)quinazolin-4-amine 256 N-(3,4-dichlorophenyl)-7-[({2-[(2S)-1-ethylpyrrolidin-2-yl]-1,3-thiazol-4- yl}methyl)oxy]-6-(methyloxy)quinazolin-4-amine 257 N-(3,4-dichlorophenyl)-7-{[(5-ethyl-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridin- 2-yl)methyl]oxy}-6-(methyloxy)quinazolin-4-amine 258 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4-propyl-1,4-oxazepan-2- yl)methyl]oxy}quinazolin-4-amine 259 7-({[4-(cyclopropylmethyl)-1,4-oxazepan-2-yl]methyl}oxy)-N-(3,4- dichlorophenyl)-6-(methyloxy)quinazolin-4-amine 260 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({4-[2-(methyloxy)ethyl]-1,4-oxazepan- 2-yl}methyl)oxy]quinazolin-4-amine 261 N-(3,4-dichlorophenyl)-7-({[4-(1-methylethyl)-1,4-oxazepan-2-yl]methyl}oxy)-6- (methyloxy)quinazolin-4-amine 262 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(2-piperazin-1-yl-1,3-thiazol-4- yl)methyl]oxy}quinazolin-4-amine 263 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(5-pyrrolidin-2-yl-1,2,4-oxadiazol-3- yl)methyl]oxy}quinazolin-4-amine 264 N-(3,4-dichlorophenyl)-7-({[5-(1-ethylpyrrolidin-2-yl)-1,2,4-oxadiazol-3- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 265 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({3-[(2S)-1-methylpyrrolidin-2-yl]- 1,2,4-oxadiazol-5-yl}methyl)oxy]quinazolin-4-amine 266 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({2-[(2S)-1-methylpyrrolidin-2-yl]-1,3- thiazol-4-yl}methyl)oxy]quinazolin-4-amine 267 N-(3,4-dichlorophenyl)-7-({[2-(4-ethylpiperazin-1-yl)-1,3-thiazol-4- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 268 N-(3,4-dichlorophenyl)-7-{[(1,4-dimethylpiperazin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 269 7-{[(4-cyclopentylmorpholin-2-yl)methyl]oxy}-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 270 N-(3,4-dichlorophenyl)-7-({[4-(1-methylethyl)morpholin-2-yl]methyl}oxy)-6- (methyloxy)quinazolin-4-amine 271 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(3-phenylpropyl)morpholin-2- yl]methyl}oxy)quinazolin-4-amine 272 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({4-[2-(methyloxy)ethyl]morpholin-2- yl}methyl)oxy]quinazolin-4-amine 273 ethyl 2-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl]propanoate 274 N-(3,4-dichlorophenyl)-7-{[(4-hex-5-en-1-ylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 275 2-({2-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl]ethyl}oxy)ethanol 276 methyl 3-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl]propanoate 277 6-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl]hexanenitrile 278 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(tetrahydro-2H-pyran-2- ylmethyl)morpholin-2-yl]methyl}oxy)quinazolin-4-amine 279 4-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl]butanenitrile 280 N-(3,4-dichlorophenyl)-7-[({4-[(4-fluorophenyl)methyl]morpholin-2- yl}methyl)oxy]-6-(methyloxy)quinazolin-4-amine 281 methyl 5-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl]pentanoate 282 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4-oct-7-en-1-ylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 283 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4-propylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 284 6-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl]hexan-1-ol 285 7-{[(4-acetylmorpholin-2-yl)methyl]oxy}-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 286 7-({[4-(cyclopropylmethyl)morpholin-2-yl]methyl}oxy)-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 287 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4-prop-2-yn-1-ylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 288 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4-pyridin-4-ylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 289 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(pyridin-2-ylmethyl)morpholin-2- yl]methyl}oxy)quinazolin-4-amine 290 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4-pent-2-yn-1-ylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 291 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[2-(4-methylpiperazin-1-yl)-1,3- thiazol-4-yl]methyl}oxy)quinazolin-4-amine 292 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[5-(1-methylpyrrolidin-2-yl)-1,2,4- oxadiazol-3-yl]methyl}oxy)quinazolin-4-amine 293 N-(3-chloro-4-fluorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 294 7-{[(4-butyl-1,4-oxazepan-2-yl)methyl]oxy}-N-(3,4-dichlorophenyl)-6- (methyloxy) quinazolin-4-amine 295 (3,4-dichlorophenyl)[7-(methyloxy)-6-({[4-(2-methylpropyl)-1,4-oxazepan-2- yl]methyl}oxy) quinazolin-4-amine 296 7-{[(4-acetyl-1-ethylpiperazin-2-yl)methyl]oxy}-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 297 (3,4-dichlorophenyl)(6-(methyloxy)-7-{[(4-pentyl-1,4-oxazepan-2-yl)methyl]oxy} quinazolin-4-amine 298 (3,4-dichlorophenyl)[6-(methyloxy)-7-({[4-(tetrahydro-2H-pyran-2-ylmethyl)-1,4- oxazepan-2-yl]methyl}oxy)quinazolin-4-amine 299 (3,4-dichlorophenyl)[6-(methyloxy)-7-({[4-(3-thienylmethyl)-1,4-oxazepan-2- yl]methyl}oxy) quinazolin-4-amine 300 N-[4-chloro-2,5-bis(methyloxy)phenyl]-7-{[(4-methylmorpholin-2- yl)methyl]oxy}-6-(methyloxy)quinazolin-4-amine 301 N-(3-bromo-2-methylphenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 302 7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6-(methyloxy)-N-(3,4,5- trichlorophenyl)quinazolin-4-amine 303 N-(3-chloro-2-methylphenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 304 N-(3,4-dichlorophenyl)-7-{[(4-ethanimidoyl-1,4-oxazepan-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 305 N-(4-bromo-2-fluorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 306 N-(5-chloro-2-fluorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 307 N-(4-chloro-2-fluorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 308 N-(2,4-dichlorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 309 N-(2,4-dibromophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 310 7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6-(methyloxy)-N-(2,3,4- trichlorophenyl)quinazolin-4-amine 311 N-(3,4-dichlorophenyl)-7-{[(1-ethyl-4-methylpiperazin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 312 N′-cyano-2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholine-4-carboximidamide 313 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[2-(pyrrolidin-1-ylmethyl)-1,3-thiazol- 4-yl]methyl}oxy)quinazolin-4-amine 314 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(tetrahydro-2H-pyran-4- yl)morpholin-2-yl]methyl}oxy)quinazolin-4-amine 315 N-(3,4-dichlorophenyl)-7-({[4-(2-ethylbutyl)morpholin-2-yl]methyl}oxy)-6- (methyloxy)quinazolin-4-amine 316 7-({[4-(cyclohexylmethyl)morpholin-2-yl]methyl}oxy)-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 317 2-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl]ethanol 318 7-{[(4-but-2-yn-1-ylmorpholin-2-yl)methyl]oxy}-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 319 7-{[(4-cyclobutylmorpholin-2-yl)methyl]oxy}-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 320 N-(3,4-dichlorophenyl)-7-[({4-[2-(1,3-dioxolan-2-yl)ethyl]morpholin-2- yl}methyl)oxy]-6-(methyloxy)quinazolin-4-amine 321 7-({[4-(2-cyclohexylethyl)morpholin-2-yl]methyl}oxy)-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 322 N-(3,4-dichlorophenyl)-7-[({4-[2-(1,3-dioxan-2-yl)ethyl]morpholin-2- yl}methyl)oxy]-6-(methyloxy)quinazolin-4-amine 323 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4-pent-4-en-1-ylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 324 N-(3,4-dichlorophenyl)-7-[({4-[(2R)-2-methylbutyl]morpholin-2-yl}methyl)oxy]- 6-(methyloxy)quinazolin-4-amine 325 N-(3,4-dichlorophenyl)-7-({[4-(4-fluorobutyl)morpholin-2-yl]methyl}oxy)-6- (methyloxy)quinazolin-4-amine 326 3-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl]butan-2-one 327 1-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl]butan-2-one 328 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4-pentylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 329 N-(3,4-dichlorophenyl)-7-{[(4-hexylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 330 N-(3,4-dichlorophenyl)-7-{[(4-heptylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 331 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4-octylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 332 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(2-phenylethyl)morpholin-2- yl]methyl}oxy)quinazolin-4-amine 333 7-{[(4-butylmorpholin-2-yl)methyl]oxy}-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 334 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4-prop-2-en-1-ylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 335 2-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl]-1-phenylethanone 336 N-(3,4-dichlorophenyl)-7-({[4-(2-fluoroethyl)morpholin-2-yl]methyl}oxy)-6- (methyloxy)quinazolin-4-amine 337 N-(3,4-dichlorophenyl)-7-({[4-(3-methylbut-2-en-1-yl)morpholin-2- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 338 7-[({4-[(2E)-3-bromoprop-2-en-1-yl]morpholin-2-yl}methyl)oxy]-N-(3,4- dichlorophenyl)-6-(methyloxy)quinazolin-4-amine 339 2-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl]acetamide 340 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({4-[3-(tetrahydro-2H-pyran-2- yloxy)propyl]-1,4-oxazepan-2-yl}methyl)oxy]quinazolin-4-amine 341 N-(3,4-dichlorophenyl)-7-({[4-(3-methylbutyl)-1,4-oxazepan-2-yl]methyl}oxy)-6- (methyloxy)quinazolin-4-amine 342 7-({[4-(cyclohexylmethyl)-1,4-oxazepan-2-yl]methyl}oxy)-4-[(3,4- dichlorophenyl)methyl]-6-(methyloxy)quinazoline 343 7-({[4-(2-cyclohexylethyl)-1,4-oxazepan-2-yl]methyl}oxy)-4-[(3,4- dichlorophenyl)methyl]-6-(methyloxy)quinazoline 345 N-(3,4-dichlorophenyl)-7-({[4-(2-ethylbutyl)-1,4-oxazepan-2-yl]methyl}oxy)-6- (methyloxy)quinazolin-4-amine 346 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(methylsulfonyl)-1,4-oxazepan-2- yl]methyl}oxy)quinazolin-4-amine 347 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(1-methylpiperidin-4-yl)morpholin- 2-yl]methyl}oxy)quinazolin-4-amine 348 N-(3-chloro-2-fluorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 349 N′-cyano-2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)-1,4-oxazepane-4-carboximidamide 350 N-(3-bromo-4-methylphenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 351 N-(3,4-dichlorophenyl)-7-{[(1,4-diethylpiperazin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 352 4-({[4-[(4-bromo-2-fluorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)-N′-cyanopiperidine-1-carboximidamide 353 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(methylsulfonyl)morpholin-2- yl]methyl}oxy)quinazolin-4-amine 354 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({4-[(phenylmethyl)sulfonyl]morpholin- 2-yl}methyl)oxy]quinazolin-4-amine 355 N-(3,4-dichlorophenyl)-7-[({4-[(4-fluorophenyl)sulfonyl]morpholin-2- yl}methyl)oxy]-6-(methyloxy)quinazolin-4-amine 356 N-(3,4-dichlorophenyl)-7-({[4-(ethylsulfonyl)morpholin-2-yl]methyl}oxy)-6- (methyloxy)quinazolin-4-amine 357 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(phenylsulfonyl)morpholin-2- yl]methyl}oxy)quinazolin-4-amine 358 7-[({4-[(3-chloropropyl)sulfonyl]morpholin-2-yl}methyl)oxy]-N-(3,4- dichlorophenyl)-6-(methyloxy)quinazolin-4-amine 359 7-({[4-(butylsulfonyl)morpholin-2-yl]methyl}oxy)-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 360 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({4-[(4- methylphenyl)sulfonyl]morpholin-2-yl}methyl)oxy]quinazolin-4-amine 361 N-(3,4-dichlorophenyl)-7-[({4-[(3,5-dimethylisoxazol-4-yl)carbonyl]morpholin-2- yl}methyl)oxy]-6-(methyloxy)quinazolin-4-amine 362 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4-{[3- (methyloxy)phenyl]acetyl}morpholin-2-yl)methyl]oxy}quinazolin-4-amine 363 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(2-methylpentanoyl)morpholin-2- yl]methyl}oxy)quinazolin-4-amine 364 7-[({4-[(4-butylphenyl)carbonyl]morpholin-2-yl}methyl)oxy]-N-(3,4- dichlorophenyl)-6-(methyloxy)quinazolin-4-amine 365 7-[({4-[(4-chlorophenyl)acetyl]morpholin-2-yl}methyl)oxy]-N-(3,4- dichlorophenyl)-6-(methyloxy)quinazolin-4-amine 366 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(2-propylpentanoyl)morpholin-2- yl]methyl}oxy)quinazolin-4-amine 367 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(4-methylpentanoyl)morpholin-2- yl]methyl}oxy)quinazolin-4-amine 368 N-(3,4-dichlorophenyl)-7-[({4-[(2,5-difluorophenyl)carbonyl]morpholin-2- yl}methyl)oxy]-6-(methyloxy)quinazolin-4-amine 369 7-({[4-(cyclopentylcarbonyl)morpholin-2-yl]methyl}oxy)-N-(3,4-dichlorophenyl)- 6-(methyloxy)quinazolin-4-amine 370 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(2-phenylbutanoyl)morpholin-2- yl]methyl}oxy)quinazolin-4-amine 371 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-[({4-[(2,3,6- trifluorophenyl)carbonyl]morpholin-2-yl}methyl)oxy]quinazolin-4-amine 372 N-(3,4-dichlorophenyl)-7-({[4-(furan-3-ylcarbonyl)morpholin-2-yl]methyl}oxy)-6- (methyloxy)quinazolin-4-amine 373 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4-propanoylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 374 N-(3,4-dichlorophenyl)-7-{[(4-hexanoylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 375 N-(3,4-dichlorophenyl)-7-({[4-(2-ethylhexanoyl)morpholin-2-yl]methyl}oxy)-6- (methyloxy)quinazolin-4-amine 376 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(3-phenylpropanoyl)morpholin-2- yl]methyl}oxy)quinazolin-4-amine 377 N-(3,4-dichlorophenyl)-7-({[4-(2,2-dimethylpropanoyl)morpholin-2- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 378 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[4-(naphthalen-1- ylcarbonyl)morpholin-2-yl]methyl}oxy)quinazolin-4-amine 379 7-[({4-[(2-chloropyridin-3-yl)carbonyl]morpholin-2-yl}methyl)oxy]-N-(3,4- dichlorophenyl)-6-(methyloxy)quinazolin-4-amine 380 7-[({4-[(6-chloropyridin-3-yl)carbonyl]morpholin-2-yl}methyl)oxy]-N-(3,4- dichlorophenyl)-6-(methyloxy)quinazolin-4-amine 381 7-({[4-(1,3-benzodioxol-5-ylcarbonyl)morpholin-2-yl]methyl}oxy)-N-(3,4- dichlorophenyl)-6-(methyloxy)quinazolin-4-amine 382 N-(3,4-dichlorophenyl)-6-[(1-methylethyl)oxy]-7-[(morpholin-2- ylmethyl)oxy]quinazolin-4-amine 383 N-(3,4-dichlorophenyl)-6-{[2-(methyloxy)ethyl]oxy}-7-[(morpholin-2- ylmethyl)oxy]quinazolin-4-amine 384 N-(3,4-dichlorophenyl)-6-(ethyloxy)-7-[(morpholin-2-ylmethyl)oxy]quinazolin-4- amine 385 N-(3,4-dichlorophenyl)-6-(ethyloxy)-7-{[(4-methylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 386 N-(4-bromo-2-methylphenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 387 N-(4-chloro-3-methylphenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 388 N′-cyano-2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)-N-methylmorpholine-4-carboximidamide 389 N-(4-bromo-3-chlorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 390 N-(3,4-dichlorophenyl)-6-[(1-methylethyl)oxy]-7-{[(4-methylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 391 N-(3,4-dichlorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6-{[2- (methyloxy)ethyl]oxy}quinazolin-4-amine 392 N-(4-bromo-2-chlorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 393 7-{[(4-acetyl-1,4-oxazepan-2-yl)methyl]oxy}-N-(3,4-dichlorophenyl)-6- (methyloxy)quinazolin-4-amine 394 4-[(3,4-dichlorophenyl)amino]-7-{[(4-methylmorpholin-2- yl)methyl]oxy}quinazolin-6-ol 395 N-(3-bromo-4-chlorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 396 3-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl]-3-oxopropanoic acid 397 methyl 4-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl]-4-oxobutanoate 398 N-(3,4-dichlorophenyl)-7-{[(4-methylmorpholin-3-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 399 N-(3-bromo-2-chlorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 400 N′-cyano-2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)-N-[2-(methyloxy)ethyl]morpholine-4-carboximidamide 401 N′-cyano-2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)-N-ethylmorpholine-4-carboximidamide 402 [(1E)-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl](piperidin-1-yl)methylidene]cyanamide 403 [(1E)-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl](pyrrolidin-1-yl)methylidene]cyanamide 404 [(1E)-[2-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)morpholin-4-yl](4-methylpiperazin-1-yl)methylidene]cyanamide 405 N-(3,4-dichlorophenyl)-7-{[(6-ethyl-4,6-dimethylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 406 N-(4-bromo-3-methylphenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 407 N-(3,4-dichlorophenyl)-7-{[(6,6-dimethylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 408 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4,6,6-trimethylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 409 N-(3,4-dichlorophenyl)-7-{[2-(5,5-dimethylmorpholin-2-yl)ethyl]oxy}-6- (methyloxy)quinazolin-4-amine 410 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[2-(4,5,5-trimethylmorpholin-2- yl)ethyl]oxy}quinazolin-4-amine 411 1,1-dimethylethyl 2-(2-{[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin- 7-yl]oxy}ethyl)-5,5-dimethylmorpholine-4-carboxylate 412 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[(4,5,5-trimethylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 413 N-(4-bromo-2,3-dichlorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 414 N-(4,5-dichloro-2-fluorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 415 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-{[2-(4,6,6-trimethylmorpholin-2- yl)ethyl]oxy}quinazolin-4-amine 416 N-(4-bromo-2,3-difluorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 417 N-(4-bromo-2,5-difluorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 418 N-(4-bromo-3,5-difluorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 419 N-(3,4-dichloro-2-methylphenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 420 N-(3,4-dichlorophenyl)-7-({[(2R,5S,6S)-5,6-dimethylmorpholin-2-yl]methyl}oxy)- 6-(methyloxy)quinazolin-4-amine 421 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[(2R,5S,6S)-4,5,6-trimethylmorpholin- 2-yl]methyl}oxy)quinazolin-4-amine 422 N-(3,4-dichlorophenyl)-6-(methyloxy)-7-({[(2S,5S,6S)-4,5,6-trimethylmorpholin- 2-yl]methyl}oxy)quinazolin-4-amine 423 N-(4-bromo-3-chloro-2-methylphenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}- 6-(methyloxy)quinazolin-4-amine 424 N-(4-bromo-5-chloro-2-fluorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}- 6-(methyloxy)quinazolin-4-amine 425 N-(4-bromo-3-chloro-2-fluorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}- 6-(methyloxy)quinazolin-4-amine 426 N-(3,4-dichloro-2-fluorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 427 N-(3-chloro-2,4-difluorophenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 428 N-(2,3-dichloro-4-methylphenyl)-7-{[(4-methylmorpholin-2-yl)methyl]oxy}-6- (methyloxy)quinazolin-4-amine 429 6-({[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin-7-yl]oxy}methyl)- 3,3,4-trimethylmorpholin-2-one 430 N-(4-bromo-2,3-dichlorophenyl)-6-(methyloxy)-7-{[(4,5,5-trimethylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 431 N-(4-bromo-5-chloro-2-fluorophenyl)-6-(methyloxy)-7-{[(4,5,5- trimethylmorpholin-2-yl)methyl]oxy}quinazolin-4-amine 432 N-(4,5-dichloro-2-fluorophenyl)-6-(methyloxy)-7-{[(4,5,5-trimethylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 433 N-(3,4-dichloro-2-fluorophenyl)-6-(methyloxy)-7-{[(4,5,5-trimethylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 434 N-(4-bromo-3-chloro-2-fluorophenyl)-6-(methyloxy)-7-{[(4,5,5- trimethylmorpholin-2-yl)methyl]oxy}quinazolin-4-amine 435 N-(3-chloro-2,4-difluorophenyl)-6-(methyloxy)-7-{[(4,5,5-trimethylmorpholin-2- yl)methyl]oxy}quinazolin-4-amine 436 (6S)-6-({[4-[(4-bromo-3-chloro-2-fluorophenyl)amino]-6-(methyloxy)quinazolin- 7-yl]oxy}methyl)-4-methylpiperazin-2-one 437 (6S)-6-({[4-[(3,4-dichloro-2-fluorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)-4-methylpiperazin-2-one 438 (6S)-6-({[4-[(4-bromo-3-chloro-2-fluorophenyl)amino]-6-(methyloxy)quinazolin- 7-yl]oxy}methyl)-1,4-dimethylpiperazin-2-one 439 (6S)-6-({[4-[(3,4-dichloro-2-fluorophenyl)amino]-6-(methyloxy)quinazolin-7- yl]oxy}methyl)-1,4-dimethylpiperazin-2-one 440 N-(4-bromo-3-chlorophenyl)-7-{[(3a′S,4R,6′S,6a′R)-2,2- dimethyltetrahydrospiro[1,3-dioxolane-4,3′-furo[3,2-b]furan]-6′-yl]oxy}-6- (methyloxy)quinazolin-4-amine 441 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-methyl-5-C-[(methyloxy)methyl]-L-glucitol 442 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-(methylsulfonyl)-L-glucitol 443 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-L-glucitol 444 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-S-methyl-5-thio-D-iditol 445 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-morpholin-4-yl-D-iditol 446 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-(4-methylpiperazin-1-yl)-D-iditol 447 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-pyrrolidin-1-yl-D-iditol 448 2-O-acetyl-1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-D-iditol 449 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-D-iditol 450 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-(methylsulfonyl)-D-iditol 451 2-amino-1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-D-iditol 452 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-(dimethylamino)-D-iditol 453 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-(diethylamino)-D-iditol 454 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-piperidin-1-yl-D-iditol 455 2-(acetylamino)-1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-D-iditol 456 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-methyl-5-C-(trifluoromethyl)-L-glucitol 457 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-[(methylsulfonyl)amino]-D-iditol 458 N-(4-bromo-3-chlorophenyl)-6-(methyloxy)-7-[(1-methylpyrrolidin-3- yl)oxy]quinazolin-4-amine 459 N-(4-bromo-3-chlorophenyl)-6-(methyloxy)-7-[(3R)-tetrahydrofuran-3- yloxy]quinazolin-4-amine 460 N-(4-bromo-3-chlorophenyl)-6-(methyloxy)-7-{[(3S,4R)-4- (methyloxy)tetrahydrofuran-3-yl]oxy}quinazolin-4-amine 461 1,4:3,6-dianhydro-2-deoxy-2-fluoro-5-O-(6-(methyloxy)-4-{[4-(4- methylpiperazin-1-yl)phenyl]amino}quinazolin-7-yl)-D-iditol 462 1,4:3,6-dianhydro-2-deoxy-2-fluoro-5-O-[4-{[3-fluoro-4-(4-methylpiperazin-1- yl)phenyl]amino}-6-(methyloxy)quinazolin-7-yl]-D-iditol 463 1,4:3,6-dianhydro-2-deoxy-5-O-[4-{[2,3-dichloro-4-(4-methylpiperazin-1- yl)phenyl]amino}-6-(methyloxy)quinazolin-7-yl]-2-fluoro-D-iditol 464 1,4:3,6-dianhydro-2-deoxy-5-O-[4-{[3,4-dichloro-2-(4-methylpiperazin-1- yl)phenyl]amino}-6-(methyloxy)quinazolin-7-yl]-2-fluoro-D-iditol 465 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-C-(trifluoromethyl)-D-glucitol 466 (3,4-dichlorophenyl)[6-(methyloxy)-7-({[4-(tetrahydrofuran-2-ylmethyl)-1,4- oxazepan-2-yl]methyl}oxy)quinazolin-4-amine 467 N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta- [c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 468 N-(4-bromo-3-chloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclo- penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 469 N-(3-chloro-2,4-difluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta- [c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 470 N-(4,5-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclo- penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 471 N-(4-bromo-5-chloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclo- penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 472 N-(4-bromo-2,3-dichlorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclo- penta[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 473 N-(3,4-dichlorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta[c]pyrrol- 5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 474 N-(3,4-dichlorophenyl)-7-[(2-{[(3-endo)-8-methyl-8-azabicyclo[3.2.1]oct-3- yl]amino}ethyl)oxy]-6-(methyloxy)quinazolin-4-amine 475 N-(3,4-dichlorophenyl)-7-({2-[(3-endo)-8-methyl-8-azabicyclo[3.2.1]oct-3- yl]ethyl}oxy)-6-(methyloxy)quinazolin-4-amine 476 N-(3,4-dichlorophenyl)-7-({[(3-endo)-8-methyl-8-azabicyclo[3.2.1]oct-3- yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine 477 N-(3,4-dichlorophenyl)-7-{[(3-exo)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl]oxy}-6- (methyloxy)quinazolin-4-amine 478 1,4:3,6-Dianhydro-5-O-[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin- 7-yl]-2-O-methyl-D-glucitol 479 1,4:3,6-dianhydro-5-O-{4-[(3-chloro-2-fluorophenyl)amino]-6-(methyloxy)quinazolin- 7-yl}-2-deoxy-2-fluoro-L-iditol 480 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-(methylsulfonyl)-D-glucitol 481 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-D-glucitol 482 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-S-methyl-5-thio-L-iditol 483 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-morpholin-4-yl-L-iditol 484 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-(4-methylpiperazin-1-yl)-L-iditol 485 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-pyrrolidin-1-yl-L-iditol 486 2-O-acetyl-1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-L-iditol 487 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-L-iditol 488 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-(methylsulfonyl)-L-iditol 489 2-amino-1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-L-iditol 490 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-(dimethylamino)-L-iditol 491 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-(diethylamino)-L-iditol 492 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-piperidin-1-yl-L-iditol 493 2-(acetylamino)-1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-L-iditol 494 1,4:3,6-dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-methyl-5-C-(trifluoromethyl)-D-glucitol 495 1,4:3,6-dianhydro-5-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-2-deoxy-2-[(methylsulfonyl)amino]-L-iditol 496 1,4:3,6-dianhydro-2-deoxy-2-fluoro-5-O-(6-(methyloxy)-4-{[4-(4- methylpiperazin-1-yl)phenyl]amino}quinazolin-7-yl)-L-iditol 497 1,4:3,6-dianhydro-2-deoxy-2-fluoro-5-O-[4-{[3-fluoro-4-(4-methylpiperazin-1- yl)phenyl]amino}-6-(methyloxy)quinazolin-7-yl]-L-iditol 498 1,4:3,6-dianhydro-2-deoxy-5-O-[4-{[2,3-dichloro-4-(4-methylpiperazin-1- yl)phenyl]amino}-6-(methyloxy)quinazolin-7-yl]-2-fluoro-L-iditol 499 1,4:3,6-dianhydro-2-deoxy-5-O-[4-{[3,4-dichloro-2-(4-methylpiperazin-1- yl)phenyl]amino}-6-(methyloxy)quinazolin-7-yl]-2-fluoro-L-iditol 500 1,4:3,6-Dianhydro-5-O-[4-[(3,4-dichlorophenyl)amino]-6-(methyloxy)quinazolin- 7-yl]-2-O-methyl-D-glucitol 501 1,4:3,6-Dianhydro-2-O-[4-[(4-bromo-3-chlorophenyl)amino]-6- (methyloxy)quinazolin-7-yl]-5-O-methyl-L-glucitol

Table 5a Representative IGF-1R Inhibitor

The Compounds in Table 5a can be prepared as pharmaceutically acceptable salts, solvates, hydrates, and/or isomers thereof. All such salt, solvate, hydrate, and isomer combinations of the Compounds in Table 5a can be used to practice the invention.

Entry Structure 1

2

3

4

5

6

7

8

9

10

11

12

13

14

15

16

17

18

19

20

21

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24

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27

28

29

30

31

32

33

34

35

36

37

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52

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90

91

92

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94

95

96

97

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106

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109

110

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112

113

114

115

116

117

118

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125

126

127

128

129

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132

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146

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149

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151

152

153

154

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211

212

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229

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239

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267

268

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286

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291

292

293

294

295

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312

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319

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321

322

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331

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343

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349

350

351

352

353

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358

495

496

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501

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510

511

512

513

514

515

516

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521

522

523

524

525

526

527

528

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531

532

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535

536

537

538

539

540

541

542

543

544

545

546

547

548

549

550

551

552

553

554

555

556

557

558

559

560

561

562

563

564

565

566

567

568

569

570

571

572

Table 5b Additional Representative IGF1R Inhibitors

The Compounds in Table 5b can be prepared as pharmaceutically acceptable salts, solvates, hydrates, and/or isomers thereof. All such salt, solvate, hydrate, and isomer combinations of the Compounds in Table 5b can be used to practice the invention.

Entry Structure Name 573

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N⁶-[3-(diethylamino)propyl]- N²-{[3-(1-methylethyl)isoxazol-5- yl]methyl}pyrimidine-2,4,6- triamine 574

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N⁶-[2-(diethylamino)ethyl]-N²- {[3-(1-methylethyl)isoxazol-5- yl]methyl}pyrimidine-2,4,6- triamine 575

N²-{[3-(1-methylethyl)isoxazol-5- yl]methyl}-N⁴-[5-(1-methylethyl)- 1H-pyrazol-3-yl]-6-[(3S)-3- methylpiperazin-1-yl]pyrimidine- 2,4-diamine 576

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-{[2- (dimethylamino)ethyl]oxy}-N²- {[3-(1-methylethyl)isoxazol-5- yl]methyl}pyrimidine-2,4-diamine 577

N⁴-[3-(1-methylethyl)-1H- pyrazol-5-yl]-6-[(1- methylpyrrolidin-3-yl)oxy]-N²- [(3-phenylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 578

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-N²-{[3-(1- methylethyl)isoxazol-5- yl]methyl}-6-[(1- methylpyrrolidin-3- yl)oxy]pyrimidine-2,4-diamine 579

N²-{[3-(1-methylethyl)isoxazol-5- yl]methyl}-N⁴-[3-(1-methylethyl)- 1H-pyrazol-5-yl]-6-[(1- methylpyrrolidin-3- yl)oxy]pyrimidine-2,4-diamine 580

N⁴-[2-(diethylamino)ethyl]-N²- {[3-(1-methylethyl)isoxazol-5- yl]methyl}-N⁶-[5-(1-methylethyl)- 1H-pyrazol-3-yl]pyrimidine-2,4,6- triamine 581

N²-{[3-(1-methylethyl)isoxazol-5- yl]methyl}-N⁴-[5-(1-methylethyl)- 1H-pyrazol-3-yl]pyrimidine-2,4- diamine 582

N⁴-[5-(1-methylethyl)-1H- pyrazol-3-yl]-6-[(1- methylpiperidin-3-yl)oxy]-N²-[(3- phenylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 583

N²-{[3-(1-methylethyl)isoxazol-5- yl]methyl}-N⁴-[5-(1-methylethyl)- 1H-pyrazol-3-yl]-6-[(1- methylpiperidin-3- yl)oxy]pyrimidine-2,4-diamine 584

N-(5-cyclopropyl-1H-pyrazol-3- yl)-6-methyl-2-{[(3- phenylisoxazol-5- yl)methyl]oxy}pyrimidin-4-amine 585

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-methyl-N²-[(4-phenyl-1H- imidazol-2-yl)methyl]pyrimidine- 2,4-diamine 586

6-{[2-(dimethylamino)ethyl]oxy}- N²-{[3-(1-methylethyl)isoxazol-5- yl]methyl}-N⁴-[5-(1-methylethyl)- 1H-pyrazol-3-yl]pyrimidine-2,4- diamine 587

N²-{[3-(1-methylethyl)isoxazol-5- yl]methyl}-N⁴-[5-(1-methylethyl)- 1H-pyrazol-3-yl]-6-[(2- morpholin-4- ylethyl)oxy]pyrimidine-2,4- diamine 588

N⁴-[5-(1-methylethyl)-1H- pyrazol-3-yl]-6-[(2-morpholin-4- ylethyl)oxy]-N²-[(3- phenylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 589

N⁴-[3-(1-methylethyl)-1H- pyrazol-5-yl]-N²-[(3- phenylisoxazol-5-yl)methyl]-6- [(2-piperidin-1- ylethyl)oxy]pyrimidine-2,4- diamine 590

N⁴-[3-(diethylamino)propyl]-N²- {[3-(1-methylethyl)isoxazol-5- yl]methyl}-N⁶-[5-(1-methylethyl)- 1H-pyrazol-3-yl]pyrimidine-2,4,6- triamine 591

N⁴-[5-(1-methylethyl)-1H- pyrazol-3-yl]-6-[(3S)-3- methylpiperazin-1-yl]-N²-[(3- phenylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 592

N⁴-[2-(diethylamino)ethyl]-N⁶-[5- (1-methylethyl)-1H-pyrazol-3-yl]- N²-[(3-phenylisoxazol-5- yl)methyl]pyrimidine-2,4,6- triamine 593

N⁴-[5-(1-methylethyl)-1H- pyrazol-3-yl]-6-[(1- methylpiperidin-4-yl)oxy]-N²-[(3- phenylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 594

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N²-{[3-(1- methylethyl)isoxazol-5- yl]methyl}-6-[(2-morpholin-4- ylethyl)oxy]pyrimidine-2,4- diamine 595

N²-{[3-(1-methylethyl)isoxazol-5- yl]methyl}-N⁴-[3-(1-methylethyl)- 1H-pyrazol-5-yl]-6-[(2-piperidin- 1-ylethyl)oxy]pyrimidine-2,4- diamine 596

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-6-[3-(diethylamino)propyl]- N²-[(3-phenylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 597

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-N²-{[3-(1- methylethyl)isoxazol-5- yl]methyl}-6-[(2-piperidin-1- ylethyl)oxy]pyrimidine-2,4- diamine 598

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N²-{[3-(1- methylethyl)isoxazol-5- yl]methyl}-6-[(1-methylpiperidin- 3-yl)oxy]pyrimidine-2,4-diamine 599

N²-{[3-(1-methylethyl)isoxazol-5- yl]methyl}-N⁴-[3-(1-methylethyl)- 1H-pyrazol-5-yl]-6-[(1- methylpiperidin-4- yl)oxy]pyrimidine-2,4-diamine 600

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-6-methyl-N²-[(3- methylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 601

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-N²-[(3-methylisoxazol-5- yl)methyl]-6-morpholin-4- ylpyrimidine-2,4-diamine 602

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-N²-[(3-methylisoxazol-5- yl)methyl]-6-(4-methylpiperazin- 1-yl)pyrimidine-2,4-diamine 603

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N²-{[3-(1- methylethyl)isoxazol-5- yl]methyl}-6-[(1-methylpiperidin- 4-yl)oxy]pyrimidine-2,4-diamine 604

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-N²-{[3-(4- fluorophenyl)isoxazol-5- yl]methyl}-6-morpholin-4- ylpyrimidine-2,4-diamine 605

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-N²-{[3-(4- fluorophenyl)isoxazol-5- yl]methyl}-6-(4-methylpiperazin- 1-yl)pyrimidine-2,4-diamine 606

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-N²-{[3-(4- fluorophenyl)isoxazol-5- yl]methyl}-6-[(2-morpholin-4- ylethyl)oxy]pyrimidine-2,4- diamine 607

N²-{[3-(4-fluorophenyl)isoxazol- 5-yl]methyl}-N⁴-[3-(1- methylethyl)-1H-pyrazol-5-yl]-6- morpholin-4-ylpyrimidine-2,4- diamine 608

N²-{[3-(4-fluorophenyl)isoxazol- 5-yl]methyl}-N⁴-[3-(1- methylethyl)-1H-pyrazol-5-yl]-6- (4-methylpiperazin-1- yl)pyrimidine-2,4-diamine 609

N²-{[3-(4-fluorophenyl)isoxazol- 5-yl]methyl}-N⁴-[3-(1- methylethyl)-1H-pyrazol-5-yl]-6- [(2-morpholin-4- ylethyl)oxy]pyrimidine-2,4- diamine 610

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-methyl-N²-[(3-pyridin-3- ylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 611

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-(4-methylpiperazin-1-yl)-N²- [(3-pyridin-2-ylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 612

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-morpholin-4-yl-N²-[(3- pyridin-2-ylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 613

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N²-{[3-(1- methylethyl)isoxazol-5- yl]methyl}-6-piperazin-1- ylpyrimidine-2,4-diamine 614

6-(4-acetylpiperazin-1-yl)-N⁴-(5- cyclopropyl-1H-pyrazol-3-yl)-N²- {[3-(1-methylethyl)isoxazol-5- yl]methyl}pyrimidine-2,4-diamine 615

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N²-{[3-(1- methylethyl)isoxazol-5- yl]methyl}-6-[4- (methylsulfonyl)piperazin-1- yl]pyrimidine-2,4-diamine 616

4-{6-[(5-cyclopropyl-1H-pyrazol- 3-yl)amino]-2-({[3-(1- methylethyl)isoxazol-5- yl]methyl}amino)pyrimidin-4- yl}piperazine-1-carbaldehyde 617

N⁴-(3-methyl-1H-pyrazol-5-yl)-6- morpholin-4-yl-N²-[(3- phenylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 618

6-(4-methylpiperazin-1-yl)-N⁴-(3- methyl-1H-pyrazol-5-yl)-N²-[(3- phenylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 619

N⁴-(3-methyl-1H-pyrazol-5-yl)-6- [(2-morpholin-4-ylethyl)oxy]-N²- [(3-phenylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 620

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-methyl-N²-[(3-pyridin-4- ylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 621

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N²-{[3-(3,4- difluorophenyl)isoxazol-5- yl]methyl}-6-methylpyrimidine- 2,4-diamine 622

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N²-{[3-(2,4- difluorophenyl)isoxazol-5- yl]methyl}-6-methylpyrimidine- 2,4-diamine 623

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-methyl-N²-[(3-pyrazin-2- ylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 624

5-chloro-N⁴-(3-cyclopropyl-1H- pyrazol-5-yl)-6-morpholin-4-yl- N²-[(3-phenylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 625

5-chloro-N⁴-(3-cyclopropyl-1H- pyrazol-5-yl)-6-(4- methylpiperazin-1-yl)-N²-[(3- phenylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 626

N²-[(3-methylisoxazol-5- yl)methyl]-6-(4-methylpiperazin- 1-yl)-N⁴-(3-methyl-1H-pyrazol-5- yl)pyrimidine-2,4-diamine 627

N²-[(3-methylisoxazol-5- yl)methyl]-N⁴-(3-methyl-1H- pyrazol-5-yl)-6-morpholin-4- ylpyrimidine-2,4-diamine 628

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-(4-methylpiperazin-1-yl)-N²- [(3-pyrimidin-4-ylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 629

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N²-[(3-furan-3-ylisoxazol-5- yl)methyl]-6-(4-methylpiperazin- 1-yl)pyrimidine-2,4-diamine 630

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N⁶-(8-methyl-8- azabicyclo[3.2.1]oct-3-yl)-N²-[(3- methylisoxazol-5- yl)methyl]pyrimidine-2,4,6- triamine 631

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-(5-methyl-2,5- diazabicyclo[2.2.1]hept-2-yl)-N²- [(3-methylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 632

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-(5-methyl-2,5- diazabicyclo[2.2.1]hept-2-yl)-N²- {[3-(1-methylethyl)isoxazol-5- yl]methyl}pyrimidine-2,4-diamine 633

N⁴-bicyclo[2.2.1]hept-2-yl-N⁶-(5- cyclopropyl-1H-pyrazol-3-yl)-N²- {[3-(1-methylethyl)isoxazol-5- yl]methyl}pyrimidine-2,4,6- triamine 634

N⁴-bicyclo[2.2.1]hept-2-yl-N⁶-(5- cyclopropyl-1H-pyrazol-3-yl)-N²- [(3-methylisoxazol-5- yl)methyl]pyrimidine-2,4,6- triamine 635

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N²-[(3-methylisoxazol-5- yl)methyl]-6-[(1R,4R)-5- (phenylmethyl)-2,5- diazabicyclo[2.2.1]hept-2- yl]pyrimidine-2,4-diamine 636

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N²-{[3-(1- methylethyl)isoxazol-5- yl]methyl}-6-[(1R,4R)-5- (phenylmethyl)-2,5- diazabicyclo[2.2.1]hept-2- yl]pyrimidine-2,4-diamine 637

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-morpholin-4-yl-N²-[(3- pyrimidin-4-ylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 638

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-{[2- (dimethylamino)ethyl]oxy}-N²- [(3-pyrimidin-4-ylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 639

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N²-{[3-(5-fluoropyridin-2- yl)isoxazol-5-yl]methyl}-6- methylpyrimidine-2,4-diamine 640

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-(4-methylpiperazin-1-yl)-N²- {[3-(2-thienyl)isoxazol-5- yl]methyl}pyrimidine-2,4-diamine 641

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-{[2- (dimethylamino)ethyl]oxy}-N²- [(3-pyridin-2-ylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 642

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-6-(4-methylpiperazin-1-yl)-N²- [(3-pyrimidin-5-ylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 643

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-6-morpholin-4-yl-N²-[(3- pyrimidin-5-ylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 644

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-{[2- (diethylamino)ethyl]oxy}-N²-{[3- (1-methylethyl)isoxazol-5- yl]methyl}pyrimidine-2,4-diamine 645

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N²-{[3-(1- methylethyl)isoxazol-5- yl]methyl}-6-[(2-pyrrolidin-1- ylethyl)oxy]pyrimidine-2,4- diamine 646

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-{[2- (diethylamino)ethyl]oxy}-N²-[(3- methylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 647

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-N²-[(3-methylisoxazol-5- yl)methyl]-6-[(2-pyrrolidin-1- ylethyl)oxy]pyrimidine-2,4- diamine 648

N⁴-(5-cyclopropyl-1H-pyrazol-3- yl)-6-(4-methylpiperazin-1-yl)-N²- {[3-(1,3-thiazol-2-yl)isoxazol-5- yl]methyl}pyrimidine-2,4-diamine 649

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-6-[2-(dimethylamino)ethoxy]- N²-[(3-methylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 650

6-{[2-(dimethylamino)ethyl]oxy}- N²-[(3-methylisoxazol-5- yl)methyl]-N⁴-(3-methyl-1H- pyrazol-5-yl)pyrimidine-2,4- diamine 651

6-{[2-(diethylamino)ethyl]oxy}- N²-[(3-methylisoxazol-5- yl)methyl]-N⁴-(3-methyl-1H- pyrazol-5-yl)pyrimidine-2,4- diamine 652

N²-[(3-methylisoxazol-5- yl)methyl]-N⁴-(3-methyl-1H- pyrazol-5-yl)-6-[(2-pyrrolidin-1- ylethyl)oxy]pyrimidine-2,4- diamine 653

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-6-methyl-N²-[2-(3- phenylisoxazol-5- yl)ethyl]pyrimidine-2,4-diamine 654

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-6-methyl-N²-[1-(3- phenylisoxazol-5- yl)ethyl]pyrimidine-2,4-diamine 655

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-N²-[(3-ethylisoxazol-5- yl)methyl]-6-(4-methylpiperazin- 1-yl)pyrimidine-2,4-diamine 656

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-N²-[(3-ethylisoxazol-5- yl)methyl]-6-morpholin-4- ylpyrimidine-2,4-diamine 657

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-6-{[2- (dimethylamino)ethyl]oxy}-N²- [(3-ethylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 658

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-6-{[2- (diethylamino)ethyl]oxy}-N²-[(3- ethylisoxazol-5- yl)methyl]pyrimidine-2,4-diamine 659

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-N²-[(3-ethylisoxazol-5- yl)methyl]-6-[(2-pyrrolidin-1- ylethyl)oxy]pyrimidine-2,4- diamine 660

N²-{[3-(2-aminopyrimidin-4- yl)isoxazol-5-yl]methyl}-N⁴-(3- cyclopropyl-1H-pyrazol-5-yl)-6- (4-methylpiperazin-1- yl)pyrimidine-2,4-diamine 661

N⁴-(3-cyclopropyl-1H-pyrazol-5- yl)-6-(4-ethylpiperazin-1-yl)-N²- {[3-(1-methylethyl)isoxazol-5- yl]methyl}pyrimidine-2,4-diamine 662

2-(1-{6-[(3-cyclopropyl-1H- pyrazol-5-yl)amino]-2-({[3-(1- methylethyl)isoxazol-5- yl]methyl}amino)pyrimidin-4- yl}piperidin-4-yl)ethanol 663

2-(4-{6-[(3-cyclopropyl-1H- pyrazol-5-yl)amino]-2-({[3-(1- methylethyl)isoxazol-5- yl]methyl}amino)pyrimidin-4- yl}piperazin-1-yl)ethanol

Table 6 Representative Raf Inhibitors

The Compounds in Table 6 can be prepared as pharmaceutically acceptable salts, solvates, hydrates, and/or isomers thereof. All such salt, solvate, hydrate, and isomer combinations of the Compounds in Table 6 can be used to practice the invention.

Entry Name 1 6-(2-butyl-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl)-2H-1,4-benzoxazin- 3(4H)-one 2 6-[1-hydroxy-3-oxo-2-(2-phenylethyl)-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 3 6-(1-hydroxy-2-{[4-(methyloxy)phenyl]methyl}-3-oxo-2,3-dihydro-1H-isoindol- 1-yl)-2H-1,4-benzoxazin-3(4H)-one 4 6-(1-hydroxy-2-{[3-(methyloxy)phenyl]methyl}-3-oxo-2,3-dihydro-1H-isoindol- 1-yl)-2H-1,4-benzoxazin-3(4H)-one 5 6-{2-[(4-fluorophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl}- 2H-1,4-benzoxazin-3(4H)-one 6 6-(1-hydroxy-3-oxo-2-phenyl-2,3-dihydro-1H-isoindol-1-yl)-2H-1,4-benzoxazin- 3(4H)-one 7 6-{2-[(3-bromophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl}- 2H-1,4-benzoxazin-3(4H)-one 8 6-{2-[(4-bromophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl}- 2H-1,4-benzoxazin-3(4H)-one 9 6-[1-hydroxy-3-oxo-2-(3-phenylpropyl)-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 10 6-{2-[(3,4-dichlorophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl}-2H-1,4-benzoxazin-3(4H)-one 11 6-{1-hydroxy-2-[(4-methylphenyl)methyl]-3-oxo-2,3-dihydro-1H-isoindol-1-yl}- 2H-1,4-benzoxazin-3(4H)-one 12 6-{2-[(4-chlorophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl}- 2H-1,4-benzoxazin-3(4H)-one 13 6-[1-hydroxy-2-(1-methylethyl)-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 14 methyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 15 6-{2-[(3,4-dimethylphenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl}-2H-1,4-benzoxazin-3(4H)-one 16 6-(2-{[4-chloro-3-(trifluoromethyl)phenyl]methyl}-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl)-2H-1,4-benzoxazin-3(4H)-one 17 6-(2-{[4-(dimethylamino)phenyl]methyl}-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl)-2H-1,4-benzoxazin-3(4H)-one 18 6-[2-(3-chlorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 19 6-[2-(4-chlorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 20 6-[2-(3,4-dichlorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H- 1,4-benzoxazin-3(4H)-one 21 6-[1-hydroxy-2-(4-methylphenyl)-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 22 3-(2-{[3,5-bis(methyloxy)phenyl]amino}-1H-benzimidazol-5-yl)-3-(methyloxy)- 2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-one 23 3-(2-{[3,5-bis(methyloxy)phenyl]amino}-1H-benzimidazol-5-yl)-2-(1- methylethyl)-3-(methyloxy)-2,3-dihydro-1H-isoindol-1-one 24 3-(2-{[3,5-bis(methyloxy)phenyl]amino}-1H-benzimidazol-5-yl)-3-hydroxy-2- phenyl-2,3-dihydro-1H-isoindol-1-one 25 3-(2-{[3,5-bis(methyloxy)phenyl]amino}-1H-benzimidazol-5-yl)-3-hydroxy-2- (phenylmethyl)-2,3-dihydro-1H-isoindol-1-one 26 methyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1- methyl-1H-benzimidazol-2-yl}carbamate 27 3-(1H-benzimidazol-5-yl)-3-hydroxy-2-(phenylmethyl)-2,3-dihydro-1H-isoindol- 1-one 28 5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-N-methyl- 1H-benzimidazole-2-carboxamide 29 3-hydroxy-3-(2-methyl-1H-benzimidazol-5-yl)-2-(phenylmethyl)-2,3-dihydro- 1H-isoindol-1-one 30 7-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-3,4- dihydroquinoxalin-2(1H)-one 31 7-[2-(3-chlorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-3,4- dihydroquinoxalin-2(1H)-one 32 1,1-dimethylethyl 4-{[1-hydroxy-3-oxo-1-(3-oxo-3,4-dihydro-2H-1,4- benzoxazin-6-yl)-1,3-dihydro-2H-isoindol-2-yl]methyl}piperidine-1-carboxylate 33 6-(1-hydroxy-2-{[2-(methyloxy)phenyl]methyl}-3-oxo-2,3-dihydro-1H-isoindol- 1-yl)-2H-1,4-benzoxazin-3(4H)-one 34 6-{2-[(3-chlorophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl}- 2H-1,4-benzoxazin-3(4H)-one 35 6-{2-[(2-chlorophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl}- 2H-1,4-benzoxazin-3(4H)-one 36 6-{2-[(3-fluorophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl}- 2H-1,4-benzoxazin-3(4H)-one 37 6-{2-[(2-bromophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl}- 2H-1,4-benzoxazin-3(4H)-one 38 6-{2-[(2-fluorophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl}- 2H-1,4-benzoxazin-3(4H)-one 39 6-[2-(3-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 40 6-[1-hydroxy-2-(3-iodophenyl)-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 41 6-[2-(3-bromophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 42 6-[1-hydroxy-2-(3-nitrophenyl)-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 43 6-{1-hydroxy-2-[3-(methyloxy)phenyl]-3-oxo-2,3-dihydro-1H-isoindol-1-yl}- 2H-1,4-benzoxazin-3(4H)-one 44 6-[1-hydroxy-2-(3-methylphenyl)-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 45 3-hydroxy-3-(1H-indol-5-yl)-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-one 46 methyl [6-(1-hydroxy-3-oxo-2-phenyl-2,3-dihydro-1H-isoindol-1-yl)-1H- benzimidazol-2-yl]carbamate 47 6-[2-(2-aminophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 48 6-{[2-(3-phenyl-1,2,4-oxadiazol-5-yl)phenyl]carbonyl}-2H-1,4-benzoxazin- 3(4H)-one 49 6-{[2-(1H-benzimidazol-2-yl)phenyl]carbonyl}-2H-1,4-benzoxazin-3(4H)-one 50 6-(1-hydroxy-3-oxo-2-{[2-(trifluoromethyl)phenyl]methyl}-2,3-dihydro-1H- isoindol-1-yl)-2H-1,4-benzoxazin-3(4H)-one 51 6-{2-[(5-bromo-2-fluorophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-2H-1,4-benzoxazin-3(4H)-one 52 6-{1-hydroxy-2-[(3-nitrophenyl)methyl]-3-oxo-2,3-dihydro-1H-isoindol-1-yl}- 2H-1,4-benzoxazin-3(4H)-one 53 6-(1-hydroxy-3-oxo-2-{[3-(trifluoromethyl)phenyl]methyl}-2,3-dihydro-1H- isoindol-1-yl)-2H-1,4-benzoxazin-3(4H)-one 54 6-(2-{[2,3-bis(methyloxy)phenyl]methyl}-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl)-2H-1,4-benzoxazin-3(4H)-one 55 6-{1-hydroxy-2-[(3-iodophenyl)methyl]-3-oxo-2,3-dihydro-1H-isoindol-1-yl}- 2H-1,4-benzoxazin-3(4H)-one 56 6-[1-hydroxy-3-oxo-2-({3-[(trifluoromethyl)oxy]phenyl}methyl)-2,3-dihydro- 1H-isoindol-1-yl]-2H-1,4-benzoxazin-3(4H)-one 57 6-(1-hydroxy-2-{[2-(methylthio)phenyl]methyl}-3-oxo-2,3-dihydro-1H-isoindol- 1-yl)-2H-1,4-benzoxazin-3(4H)-one 58 6-[2-(3,4-difluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H- 1,4-benzoxazin-3(4H)-one 59 6-{1-hydroxy-2-[3-(1-methylethyl)phenyl]-3-oxo-2,3-dihydro-1H-isoindol-1- yl}-2H-1,4-benzoxazin-3(4H)-one 60 6-(1-hydroxy-3-oxo-2-{3-[(trifluoromethyl)oxy]phenyl}-2,3-dihydro-1H- isoindol-1-yl)-2H-1,4-benzoxazin-3(4H)-one 61 6-{1-hydroxy-3-oxo-2-[3-(trifluoromethyl)phenyl]-2,3-dihydro-1H-isoindol-1- yl}-2H-1,4-benzoxazin-3(4H)-one 62 3-[1-hydroxy-3-oxo-1-(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)-1,3-dihydro- 2H-isoindol-2-yl]benzenesulfonamide 63 6-{2-[5-chloro-2-(methyloxy)phenyl]-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol- 1-yl}-2H-1,4-benzoxazin-3(4H)-one 64 6-{2-[4-fluoro-3-(trifluoromethyl)phenyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-2H-1,4-benzoxazin-3(4H)-one 65 3-hydroxy-3-(1H-indol-6-yl)-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-one 66 6-[2-(3-fluoro-5-iodophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 2H-1,4-benzoxazin-3(4H)-one 67 6-[2-(3-aminophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 68 6-[2-(3,5-difluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H- 1,4-benzoxazin-3(4H)-one 69 6-{1-hydroxy-2-[3-(methylsulfonyl)phenyl]-3-oxo-2,3-dihydro-1H-isoindol-1- yl}-2H-1,4-benzoxazin-3(4H)-one 70 ethyl 3-[1-hydroxy-3-oxo-1-(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)-1,3- dihydro-2H-isoindol-2-yl]benzoate 71 3-[1-hydroxy-3-oxo-1-(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)-1,3-dihydro- 2H-isoindol-2-yl]benzonitrile 72 6-[2-(2-chlorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 73 6-[2-(3-amino-5-chlorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 2H-1,4-benzoxazin-3(4H)-one 74 6-[2-(5-chloro-2-methylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 2H-1,4-benzoxazin-3(4H)-one 75 6-[2-(3-chloro-2-methylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 2H-1,4-benzoxazin-3(4H)-one 76 6-[2-(3-ethylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 77 6-[2-(3-ethynylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 78 6-[1-hydroxy-2-(3-hydroxyphenyl)-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 79 6-{1-hydroxy-3-oxo-2-[3-(phenyloxy)phenyl]-2,3-dihydro-1H-isoindol-1-yl}- 2H-1,4-benzoxazin-3(4H)-one 80 6-(1-hydroxy-3-oxo-2-{3-[(phenylmethyl)oxy]phenyl}-2,3-dihydro-1H-isoindol- 1-yl)-2H-1,4-benzoxazin-3(4H)-one 81 3-[1-hydroxy-3-oxo-1-(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)-1,3-dihydro- 2H-isoindol-2-yl]benzamide 82 6-{1-hydroxy-2-[3-(hydroxymethyl)phenyl]-3-oxo-2,3-dihydro-1H-isoindol-1- yl}-2H-1,4-benzoxazin-3(4H)-one 83 6-[2-(2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 84 3-hydroxy-3-[2-(methylamino)-1H-benzimidazol-5-yl]-2-(phenylmethyl)-2,3- dihydro-1H-isoindol-1-one 85 6-(2-biphenyl-3-yl-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl)-2H-1,4- benzoxazin-3(4H)-one 86 6-(2-{3-[(dimethylamino)methyl]phenyl}-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl)-2H-1,4-benzoxazin-3(4H)-one 87 6-[2-(3,5-dichlorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H- 1,4-benzoxazin-3(4H)-one 88 6-(1-hydroxy-3-oxo-2-piperidin-4-yl-2,3-dihydro-1H-isoindol-1-yl)-2H-1,4- benzoxazin-3(4H)-one 89 6-[2-(3-{[2-(dimethylamino)ethyl]oxy}phenyl)-1-hydroxy-3-oxo-2,3-dihydro- 1H-isoindol-1-yl]-2H-1,4-benzoxazin-3(4H)-one 90 6-[1-hydroxy-2-(2-methylphenyl)-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-2H-1,4- benzoxazin-3(4H)-one 91 N-methyl-2-[(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)carbonyl]-N- phenylbenzamide 92 methyl {5-[1-(ethyloxy)-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 93 phenylmethyl 2-[(2-{[(methyloxy)carbonyl]amino}-1H-benzimidazol-5- yl)carbonyl]benzoate 94 3-hydroxy-3-(1H-indazol-5-yl)-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-one 95 3-hydroxy-3-(1H-indazol-6-yl)-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-one 96 ethyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}carbamate 97 2-methylpropyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 98 methyl {5-[1-hydroxy-3-oxo-2-(2-thienylmethyl)-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 99 methyl {5-[1-hydroxy-3-oxo-2-(2-phenylethyl)-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 100 3-[2-amino-1-(1,1-dimethylethyl)-1H-benzimidazol-5-yl]-3-hydroxy-2- (phenylmethyl)-2,3-dihydro-1H-isoindol-1-one 101 3-(2-amino-1H-benzimidazol-5-yl)-3-hydroxy-2-(phenylmethyl)-2,3-dihydro- 1H-isoindol-1-one 102 methyl [5-(1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl)-1H-benzimidazol-2- yl]carbamate 103 3-(methyloxy)butyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 104 methyl (5-{1-hydroxy-3-oxo-2-[(1R)-1-phenylethyl]-2,3-dihydro-1H-isoindol-1- yl}-1H-benzimidazol-2-yl)carbamate 105 methyl (5-{1-hydroxy-3-oxo-2-[(1S)-1-phenylethyl]-2,3-dihydro-1H-isoindol-1- yl}-1H-benzimidazol-2-yl)carbamate 106 2-(methyloxy)ethyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 107 methyl {6-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1- methyl-1H-benzimidazol-2-yl}carbamate 108 prop-2-yn-1-yl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol- 1-yl]-1H-benzimidazol-2-yl}carbamate 109 but-2-yn-1-yl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol- 1-yl]-1H-benzimidazol-2-yl}carbamate 110 1-methylethyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol- 1-yl]-1H-benzimidazol-2-yl}carbamate 111 methyl {5-[2-(2,3-dihydro-1H-inden-2-yl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 112 methyl {5-[1-hydroxy-3-oxo-2-(pyridin-4-ylmethyl)-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 113 methyl {5-[1-hydroxy-3-oxo-2-(pyridin-3-ylmethyl)-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 114 methyl (6-{2-[(3-fluorophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 115 methyl {5-[1-hydroxy-2-(3-methylphenyl)-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 116 methyl [5-(1-hydroxy-2-{[2-(methyloxy)phenyl]methyl}-3-oxo-2,3-dihydro-1H- isoindol-1-yl)-1H-benzimidazol-2-yl]carbamate 117 methyl [5-(1-hydroxy-2-{[3-(methyloxy)phenyl]methyl}-3-oxo-2,3-dihydro-1H- isoindol-1-yl)-1H-benzimidazol-2-yl]carbamate 118 methyl [5-(1-hydroxy-2-{[4-(methyloxy)phenyl]methyl}-3-oxo-2,3-dihydro-1H- isoindol-1-yl)-1H-benzimidazol-2-yl]carbamate 119 methyl (6-{2-[(4-fluorophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 120 methyl (6-{2-[(3-bromophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 121 methyl (5-{1-hydroxy-2-[(3-iodophenyl)methyl]-3-oxo-2,3-dihydro-1H-isoindol- 1-yl}-1H-benzimidazol-2-yl)carbamate 122 methyl (5-{2-[(3-chlorophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 123 methyl (5-{2-[(2-fluorophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 124 methyl {5-[1-hydroxy-3-oxo-2-(pyridin-2-ylmethyl)-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 125 phenylmethyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol- 1-yl]-1H-benzimidazol-2-yl}carbamate 126 2-fluoroethyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 127 propyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 128 methyl (5-{1-hydroxy-2-[4-(methyloxy)phenyl]-3-oxo-2,3-dihydro-1H-isoindol- 1-yl}-1H-benzimidazol-2-yl)carbamate 129 methyl (5-{2-[(2-chlorophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 130 methyl (5-{2-[(2-bromophenyl)methyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 131 methyl (5-{1-hydroxy-2-[(3-methylphenyl)methyl]-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 132 methyl (5-{1-hydroxy-2-[(4-methylphenyl)methyl]-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 133 methyl (5-{1-hydroxy-2-[(2-methylphenyl)methyl]-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 134 methyl {5-[2-(3-bromophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 135 methyl {5-[2-(3-chlorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 136 methyl {5-[2-(3-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 137 methyl (5-{1-hydroxy-2-[3-(methyloxy)phenyl]-3-oxo-2,3-dihydro-1H-isoindol- 1-yl}-1H-benzimidazol-2-yl)carbamate 138 methyl {5-[2-(4-bromophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 139 methyl {5-[2-(4-chlorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 140 methyl {5-[2-(4-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 141 methyl {5-[2-(3,5-dimethylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 142 methyl {5-[2-(2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 143 methyl {5-[2-(2-chlorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 144 methyl {5-[1-hydroxy-2-(2-methylphenyl)-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 145 methyl (5-{1-hydroxy-2-[2-(methyloxy)phenyl]-3-oxo-2,3-dihydro-1H-isoindol- 1-yl}-1H-benzimidazol-2-yl)carbamate 146 methyl {5-[1-hydroxy-2-(4-methylphenyl)-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 147 methyl (5-{1-hydroxy-3-oxo-2-[3-(trifluoromethyl)phenyl]-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 148 but-2-yn-1-yl (5-{1-hydroxy-3-oxo-2-[(1R)-1-phenylethyl]-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 149 N-ethyl-N′-{5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}urea 150 phenylmethyl (5-{1-hydroxy-3-oxo-2-[(1R)-1-phenylethyl]-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 151 methyl {6-[2-(3-amino-5-chlorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 152 piperidin-4-ylmethyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 153 methyl {5-[2-(cyclopropylmethyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 154 methyl {5-[2-(2,2-dimethylpropyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 155 methyl {5-[2-(3,5-dichlorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 156 methyl {5-[2-(3,5-difluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 157 N-ethyl-N′-(5-{1-hydroxy-3-oxo-2-[(1R)-1-phenylethyl]-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)urea 158 N′-{5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}-N,N-dimethylurea 159 methyl {5-[2-(3-{[2-(dimethylamino)ethyl]oxy}phenyl)-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 160 3-(4-methylpiperazin-1-yl)propyl {6-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 161 methyl {5-[2-(cyclohexylmethyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 162 methyl {5-[1-hydroxy-2-(2-methylpropyl)-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 163 methyl {5-[1-hydroxy-3-oxo-2-(1,3-thiazol-2-ylmethyl)-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 164 methyl {5-[2-(3,4-difluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 165 methyl (5-{2-[1-(3,5-difluorophenyl)ethyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 166 methyl (5-{2-[1-(3-fluorophenyl)ethyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 167 methyl [5-(2-cyclohexyl-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl)-1H- benzimidazol-2-yl]carbamate 168 methyl {5-[2-(2,5-difluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 169 N-{5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}-N′-(phenylmethyl)urea 170 piperidin-4-yl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol- 1-yl]-1H-benzimidazol-2-yl}carbamate 171 N-{5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}-N′-methylurea 172 methyl (5-{2-[1-(2-fluorophenyl)ethyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 173 methyl (5-{1-hydroxy-3-oxo-2-[1-(2-thienyl)ethyl]-2,3-dihydro-1H-isoindol-1- yl}-1H-benzimidazol-2-yl)carbamate 174 methyl (5-{2-[1-(3-chlorophenyl)ethyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 175 methyl (5-{1-hydroxy-2-[3-methyl-5-(trifluoromethyl)phenyl]-3-oxo-2,3- dihydro-1H-isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 176 N-{5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}propanamide 177 methyl {5-[2-(3,4-dichlorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 178 methyl {5-[2-(3-ethylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 179 methyl {5-[2-(3-ethynylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 180 methyl {5-[2-(4-chloro-3-methylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 181 methyl [5-(1-hydroxy-3-oxo-2-{1-[3-(trifluoromethyl)phenyl]ethyl}-2,3-dihydro- 1H-isoindol-1-yl)-1H-benzimidazol-2-yl]carbamate 182 methyl (5-{1-hydroxy-3-oxo-2-[(1R)-1-phenylpropyl]-2,3-dihydro-1H-isoindol- 1-yl}-1H-benzimidazol-2-yl)carbamate 183 methyl [5-(1-hydroxy-3-oxo-2-{2-[(trifluoromethyl)oxy]phenyl}-2,3-dihydro- 1H-isoindol-1-yl)-1H-benzimidazol-2-yl]carbamate 184 methyl {5-[2-(2,3-difluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 185 cyclohexyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 186 tetrahydrofuran-2-ylmethyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro- 1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 187 cyclopropylmethyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 188 N-{5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}morpholine-4-carboxamide 189 methyl {5-[2-(cyclopentylmethyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 190 methyl {5-[2-(2,3-dimethylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 191 methyl {5-[2-(2,3-dihydro-1H-inden-1-yl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 192 methyl (2S)-cyclohexyl[1-hydroxy-1-(2-{[(methyloxy)carbonyl]amino}-1H- benzimidazol-5-yl)-3-oxo-1,3-dihydro-2H-isoindol-2-yl]ethanoate 193 methyl {5-[2-(2,6-difluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 194 methyl {5-[2-(3-chloro-4-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 195 but-3-en-1-yl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 196 2,2,2-trifluoroethyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 197 methyl {5-[2-(5-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 198 methyl (5-{2-[1-(5-chloro-2-methylphenyl)ethyl]-1-hydroxy-3-oxo-2,3-dihydro- 1H-isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 199 methyl (5-{1-hydroxy-3-oxo-2-[(1S)-1-phenylpropyl]-2,3-dihydro-1H-isoindol- 1-yl}-1H-benzimidazol-2-yl)carbamate 200 methyl (5-{2-[1-(3-chloro-2-methylphenyl)ethyl]-1-hydroxy-3-oxo-2,3-dihydro- 1H-isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 201 methyl (5-{1-hydroxy-2-[1-(5-methyl-2-thienyl)ethyl]-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 202 methyl (5-{2-[1-(5-chloro-2-thienyl)ethyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 203 methyl {5-[1-hydroxy-2-(3-iodophenyl)-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 204 methyl (5-{1-hydroxy-2-[3-(1-methylethyl)phenyl]-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 205 methyl {5-[2-(furan-2-ylmethyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 206 methyl {5-[1-hydroxy-3-oxo-2-(3-thienylmethyl)-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 207 methyl {5-[2-(cyclobutylmethyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 208 3,3,3-trifluoro-2-hydroxy-N-{5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro- 1H-isoindol-1-yl]-1H-benzimidazol-2-yl}-2-(trifluoromethyl)propanamide 209 methyl (5-{1-hydroxy-2-[1-(4-methyl-2-thienyl)ethyl]-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 210 methyl (5-{2-[1-(4-bromo-2-thienyl)ethyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 211 methyl {5-[1-hydroxy-2-(3-{[2-(methyloxy)ethyl]oxy}phenyl)-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 212 tetrahydrofuran-3-ylmethyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro- 1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 213 N-{5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}piperidine-1-carboxamide 214 methyl {5-[2-(3-bromo-4-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 215 2,3-dihydroxypropyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 216 methyl {5-[1-hydroxy-3-oxo-2-(tetrahydrofuran-2-ylmethyl)-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 217 methyl (5-{2-[3-(aminocarbonyl)phenyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 218 4,4,4-trifluoro-3-hydroxy-N-{5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro- 1H-isoindol-1-yl]-1H-benzimidazol-2-yl}-3-(trifluoromethyl)butanamide 219 methyl (5-{1-hydroxy-2-[3-(methylsulfonyl)phenyl]-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 220 methyl (5-{1-hydroxy-3-oxo-2-[3-(phenyloxy)phenyl]-2,3-dihydro-1H-isoindol- 1-yl}-1H-benzimidazol-2-yl)carbamate 221 methyl [5-(1-hydroxy-3-oxo-2-{3-[(phenylmethyl)oxy]phenyl}-2,3-dihydro-1H- isoindol-1-yl)-1H-benzimidazol-2-yl]carbamate 222 methyl [5-(2-biphenyl-3-yl-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl)-1H- benzimidazol-2-yl]carbamate 223 2,2-dimethyl-3-[(phenylmethyl)oxy]propyl {5-[1-hydroxy-3-oxo-2- (phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 224 methyl {5-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 225 methyl {5-[2-(3-cyanophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 226 methyl {5-[2-(3-ethynyl-4-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 227 methyl {5-[2-(4-fluoro-3-methylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 228 methyl {6-[2-(3,4-dichloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 229 [(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl {5-[1-hydroxy-3-oxo-2- (phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 230 methyl {5-[2-(5-bromo-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 231 methyl (5-{2-[3-(acetylamino)phenyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 232 methyl (5-{1-hydroxy-3-oxo-2-[3-(phenylmethyl)phenyl]-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 233 methyl (5-{2-[1-(4-chloro-2-thienyl)ethyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 234 methyl (5-{1-hydroxy-3-oxo-2-[3-(phenylcarbonyl)phenyl]-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 235 methyl [5-(2-{3-[(dimethylamino)methyl]phenyl}-1-hydroxy-3-oxo-2,3-dihydro- 1H-isoindol-1-yl)-1H-benzimidazol-2-yl]carbamate 236 methyl (5-{2-[3-(aminosulfonyl)phenyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 237 methyl {5-[2-(3-acetylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 238 methyl {5-[2-(3-ethyl-4-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 239 methyl {5-[2-(3-chloro-5-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 240 N-{6-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}-2-methylpropanamide 241 methyl (5-{2-[1-(3-chloro-2-thienyl)ethyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 242 methyl [5-(1-hydroxy-3-oxo-2-pyridin-3-yl-2,3-dihydro-1H-isoindol-1-yl)-1H- benzimidazol-2-yl]carbamate 243 methyl (5-{1-hydroxy-3-oxo-2-[3-(phenylamino)phenyl]-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 244 methyl {5-[2-(5-bromo-2,4-difluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 245 methyl {5-[2-(5-chloro-2,4-difluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 246 methyl {5-[2-(3,5-dichloro-4-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 247 2,2-dimethyl-3-(methyloxy)propyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 248 3-hydroxy-2,2-dimethylpropyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 249 methyl (5-{2-[1-(5-bromo-2-thienyl)ethyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 250 methyl {5-[2-(4,5-dichloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 251 methyl {5-[2-(3-bromo-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 252 methyl {5-[2-(3-chloro-2,4-difluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 253 N-{6-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}pent-4-ynamide 254 methyl (6-{1-methyl-3-oxo-2-[3-(trifluoromethyl)phenyl]-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 255 methyl [5-(1-hydroxy-3-oxo-2-{3-[(1,1,2,2-tetrafluoroethyl)oxy]phenyl}-2,3- dihydro-1H-isoindol-1-yl)-1H-benzimidazol-2-yl]carbamate 256 methyl {5-[1-hydroxy-3-oxo-2-(3-piperidin-4-ylphenyl)-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 257 methyl {5-[2-(3-ethenylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 258 methyl (5-{2-[3-(dimethylamino)phenyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 259 2,2-difluoro-N-{6-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol- 1-yl]-1H-benzimidazol-2-yl}cyclopropanecarboxamide 260 N-ethyl-N′-{6-[2-(4-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}urea 261 methyl {5-[2-(3-aminophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 262 N-{5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}-4-[(phenylmethyl)oxy]butanamide 263 N-{5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}-4-piperidin-1-ylbutanamide 264 N-{5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}-4-(4-methylpiperazin-1-yl)butanamide 265 N-{6-[2-(4-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}butanamide 266 methyl {6-[2-(3-bromophenyl)-5,6-dichloro-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 267 methyl [5-(1-hydroxy-2-{3-[methyl(phenyl)amino]phenyl}-3-oxo-2,3-dihydro- 1H-isoindol-1-yl)-1H-benzimidazol-2-yl]carbamate 268 methyl {5-[1-hydroxy-3-oxo-2-(phenylsulfonyl)-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 269 methyl {5-[(2-{[(phenylamino)carbonyl]amino}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 270 methyl (5-{[2-({[(phenylmethyl)oxy]carbonyl}amino)phenyl]carbonyl}-1H- benzimidazol-2-yl)carbamate 271 methyl [5-({2-[(2-phenylhydrazino)carbonyl]phenyl}carbonyl)-1H- benzimidazol-2-yl]carbamate 272 methyl {5-[(2-{[(phenyloxy)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 273 but-2-yn-1-yl {5-[2-(4-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol- 1-yl]-1H-benzimidazol-2-yl}carbamate 274 N-{5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}-3-piperidin-1-ylpropanamide 275 N-{6-[2-(4-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}propanamide 276 N-(4-fluorophenyl)-2-{[2-(pent-4-ynoylamino)-1H-benzimidazol-6- yl]carbonyl}benzamide 277 4-(diethylamino)-N-{5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}butanamide 278 N-{5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}-4-pyrrolidin-1-ylbutanamide 279 3-piperidin-1-ylpropyl {6-[2-(4-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 280 3-(4-methylpiperazin-1-yl)propyl {6-[2-(4-fluorophenyl)-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 281 methyl {5-[2-(3-bromophenyl)-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}carbamate 282 methyl {5-[2-(3-ethynyl-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 283 2-piperidin-1-ylethyl {5-[2-(4-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 284 methyl {5-[2-(3-chloro-2-methylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 285 methyl {5-[2-(5-chloro-2-methylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 286 N-{6-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}-2,2-dimethyl-3-piperidin-1-ylpropanamide 287 N-{5-[2-(4-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-1H- benzimidazol-2-yl}-4-piperidin-1-ylbutanamide 288 N-{5-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}-4-piperidin-1-ylbutanamide 289 methyl [6-({2-[(phenylcarbonyl)amino]phenyl}carbonyl)-1H-benzimidazol-2- yl]carbamate 290 methyl {5-[1-hydroxy-2-(3-morpholin-4-ylphenyl)-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 291 2-(dimethylamino)ethyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 292 2-(diethylamino)ethyl {5-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 293 2-piperidin-1-ylethyl {5-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 294 3-piperidin-1-ylpropyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 295 2-piperidin-1-ylethyl {6-[2-(3-bromophenyl)-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 296 methyl {6-[2-(3-bromophenyl)-4,7-difluoro-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 297 2-[methyl(phenylmethyl)amino]ethyl {5-[2-(3-chloro-2-fluorophenyl)-1- hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 298 methyl {5-[1-hydroxy-3-oxo-2-(3-pyrrolidin-1-ylphenyl)-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 299 methyl {5-[2-(5-chloro-2,3-difluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 300 methyl {5-[1-hydroxy-3-oxo-2-(pyrrolidin-2-ylmethyl)-2,3-dihydro-1H-isoindol- 1-yl]-1H-benzimidazol-2-yl}carbamate 301 methyl {5-[1-hydroxy-3-oxo-2-(pyrrolidin-3-ylmethyl)-2,3-dihydro-1H-isoindol- 1-yl]-1H-benzimidazol-2-yl}carbamate 302 (1-methylpiperidin-2-yl)methyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3- oxo-2,3-dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 303 [(2S)-1-methylpyrrolidin-2-yl]methyl {6-[2-(3-chloro-2-fluorophenyl)-1- hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 304 octahydro-2H-quinolizin-1-ylmethyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy- 3-oxo-2,3-dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 305 methyl {5-[2-(5-bromo-2-methylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 306 5-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1,3-dihydro-2H-benzimidazol-2-one 307 methyl {5-[2-(3-bromo-2,5-difluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 308 2-morpholin-4-ylethyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 309 (1-methylpiperidin-3-yl)methyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3- oxo-2,3-dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 310 methyl (5-{2-[5-chloro-2-(methyloxy)phenyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 311 methyl [5-(2-{3-[cyclohexyl(methyl)amino]phenyl}-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl)-1H-benzimidazol-2-yl]carbamate 312 8-azabicyclo[3.2.1]oct-3-ylmethyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3- oxo-2,3-dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 313 methyl {6-[1-(3-bromophenyl)-5-oxopyrrolidin-2-yl]-1H-benzimidazol-2- yl}carbamate 314 (1-methylpiperidin-4-yl)methyl {5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 315 1,1-dimethylethyl 4-({[({5-[1-hydroxy-3-oxo-2-(phenylmethyl)-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}amino)carbonyl]oxy}methyl)piperidine-1- carboxylate 316 (1-methylpiperidin-4-yl)methyl {5-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3- oxo-2,3-dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 317 2-(1-methylpiperidin-4-yl)ethyl {5-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3- oxo-2,3-dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 318 methyl ({6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}amino)(oxo)acetate 319 N-(5-{1-hydroxy-3-oxo-2-[3-(phenyloxy)phenyl]-2,3-dihydro-1H-isoindol-1-yl}- 1H-benzimidazol-2-yl)-4-piperidin-1-ylbutanamide 320 methyl {6-[2-(3-bromophenyl)-1-methyl-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 321 4-(diethylamino)but-2-yn-1-yl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3- oxo-2,3-dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 322 methyl {5-[2-(3-chloro-2,6-difluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 323 2-(2-oxopyrrolidin-1-yl)ethyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo- 2,3-dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 324 2-(2,5-dioxopyrrolidin-1-yl)ethyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3- oxo-2,3-dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 325 2,2,3,3-tetrafluorocyclobutyl {5-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo- 2,3-dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 326 1-acetyl-N-{5-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}piperidine-4-carboxamide 327 N-{5-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}cyclobutanecarboxamide 328 methyl [5-(2-{3-[ethyl(phenyl)amino]phenyl}-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl)-1H-benzimidazol-2-yl]carbamate 329 N-{6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}-2,2-difluorocyclopropanecarboxamide 330 cyclobutyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 331 2,2-difluoroethyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro- 1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 332 2-(3-chloro-2-fluorophenyl)-3-hydroxy-3-[2-(pyridin-2-ylamino)-1H- benzimidazol-5-yl]-2,3-dihydro-1H-isoindol-1-one 333 1-methylethyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro- 1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 334 cyclopropylmethyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 335 N-{5-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}cyclopropanecarboxamide 336 2-(methyloxy)ethyl {5-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 337 tetrahydrofuran-2-ylmethyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo- 2,3-dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 338 N-{5-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}-2-(2-thienyl)acetamide 339 methyl {6-[2-(3-chloro-2-fluorophenyl)-4,7-difluoro-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 340 ethyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 341 2-fluoroethyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 342 methyl (5-{1-hydroxy-3-oxo-2-[2-(phenyloxy)phenyl]-2,3-dihydro-1H-isoindol- 1-yl}-1H-benzimidazol-2-yl)carbamate 343 N′-{5-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}-N,N-diethylpentanediamide 344 cyclobutylmethyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro- 1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 345 2,2,2-trifluoroethyl {6-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 346 methyl (5-{2-[3-(1,1-dimethylethyl)phenyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 347 methyl {6-[2-(3-chloro-2-fluorophenyl)-7-fluoro-1-hydroxy-3-oxo-2,3-dihydro- 1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 348 2-(3-chloro-2-fluorophenyl)-3-hydroxy-3-[2-(phenylamino)-1H-benzimidazol-5- yl]-2,3-dihydro-1H-isoindol-1-one 349 methyl {6-[4,7-dichloro-2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 350 phenylmethyl 2-[(2-{[(ethyloxy)carbonyl]amino}-1,3-benzoxazol-5- yl)carbonyl]benzoate 351 methyl {5-[2-(5-chloro-3-ethynyl-2-methylphenyl)-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 352 methyl {5-[2-(5-ethynyl-2,4-difluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 353 methyl {5-[2-(3-ethynyl-2,4-difluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 354 2-(3-chloro-2-fluorophenyl)-3-hydroxy-3-[2-(pyrimidin-2-ylamino)-1H- benzimidazol-5-yl]-2,3-dihydro-1H-isoindol-1-one 355 methyl {5-[2-(3-ethynyl-2-fluorophenyl)-4,7-difluoro-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 356 2-(3-chloro-2-fluorophenyl)-3-hydroxy-3-[2-(1,3-thiazol-2-ylamino)-1H- benzimidazol-5-yl]-2,3-dihydro-1H-isoindol-1-one 357 ethyl {5-[2-(3-chloro-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1,3-benzoxazol-2-yl}carbamate 358 methyl {5-[2-(5-chloro-3-iodo-2-methylphenyl)-1-hydroxy-3-oxo-2,3-dihydro- 1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 359 methyl {5-[2-(3-ethyl-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 360 methyl {5-[2-(5-ethynyl-2-methylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 361 2-(3-chloro-2-fluorophenyl)-3-hydroxy-3-[2-(pyrazin-2-ylamino)-1H- benzimidazol-5-yl]-2,3-dihydro-1H-isoindol-1-one 362 methyl {5-[2-(2-fluoro-3-iodophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 363 methyl {6-[2-(5-ethynyl-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 364 2-(3-ethynyl-2-fluorophenyl)-3-hydroxy-3-[2-(pyrimidin-2-ylamino)-1H- benzimidazol-5-yl]-2,3-dihydro-1H-isoindol-1-one 365 methyl {5-[2-(2,5-dimethylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H-isoindol-1- yl]-1H-benzimidazol-2-yl}carbamate 366 methyl {5-[2-(3-ethenyl-2-fluorophenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 367 methyl (6-{2-[2-fluoro-3-(methyloxy)phenyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 368 methyl (5-{1-hydroxy-2-[2-methyl-5-(methyloxy)phenyl]-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 369 methyl {5-[2-(3-ethynyl-2-fluorophenyl)-7-fluoro-1-hydroxy-3-oxo-2,3-dihydro- 1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 370 methyl {5-[2-(2-fluoro-3-prop-1-yn-1-ylphenyl)-1-hydroxy-3-oxo-2,3-dihydro- 1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 371 methyl {5-[2-(5-chloro-2-methylphenyl)-7-fluoro-1-hydroxy-3-oxo-2,3-dihydro- 1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 372 methyl {5-[2-(3-ethynyl-2-methylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 373 3-hydroxy-2-[3-(methyloxy)phenyl]-3-[2-(pyrimidin-2-ylamino)-1H- benzimidazol-6-yl]-2,3-dihydro-1H-isoindol-1-one 374 3-hydroxy-2-(3-methylphenyl)-3-[2-(pyrimidin-2-ylamino)-1H-benzimidazol-6- yl]-2,3-dihydro-1H-isoindol-1-one 375 2-(5-chloro-2-methylphenyl)-3-hydroxy-3-[2-(pyrimidin-2-ylamino)-1H- benzimidazol-6-yl]-2,3-dihydro-1H-isoindol-1-one 376 methyl {6-[2-(5-chloro-2-methylphenyl)-4,7-difluoro-1-hydroxy-3-oxo-2,3- dihydro-1H-isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 377 methyl {5-[2-(3-ethynyl-2-fluorophenyl)-3-oxo-2,3-dihydro-1H-isoindol-1-yl]- 1H-benzimidazol-2-yl}carbamate 378 2-(3-chloro-2-fluorophenyl)-3-{2-[(6-chloropyridazin-3-yl)amino]-1H- benzimidazol-5-yl}-3-hydroxy-2,3-dihydro-1H-isoindol-1-one 379 2-(3-chloro-2-fluorophenyl)-4,7-difluoro-3-hydroxy-3-[2-(pyrimidin-2-ylamino)- 1H-benzimidazol-5-yl]-2,3-dihydro-1H-isoindol-1-one 380 methyl {5-[2-(2-fluoro-5-methylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 381 methyl (5-{2-[2-fluoro-5-(methyloxy)phenyl]-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 382 methyl (5-{1-hydroxy-2-[5-methyl-2-(methyloxy)phenyl]-3-oxo-2,3-dihydro-1H- isoindol-1-yl}-1H-benzimidazol-2-yl)carbamate 383 methyl {5-[2-(3-ethynyl-5-methylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 384 2-(3-chloro-2-fluorophenyl)-3-{2-[(5-chloropyrimidin-2-yl)amino]-1H- benzimidazol-5-yl}-3-hydroxy-2,3-dihydro-1H-isoindol-1-one 385 2-(3-chloro-2-fluorophenyl)-3-hydroxy-3-{2-[(4-methylpyrimidin-2-yl)amino]- 1H-benzimidazol-5-yl}-2,3-dihydro-1H-isoindol-1-one 386 3-(2-{[4,6-bis(methyloxy)pyrimidin-2-yl]amino}-1H-benzimidazol-5-yl)-2-(3- chloro-2-fluorophenyl)-3-hydroxy-2,3-dihydro-1H-isoindol-1-one 387 2-(3-chloro-2-fluorophenyl)-3-hydroxy-3-(2-{[4-methyl-6- (methyloxy)pyrimidin-2-yl]amino}-1H-benzimidazol-5-yl)-2,3-dihydro-1H- isoindol-1-one 388 3-hydroxy-2-(3-methylphenyl)-3-[2-(pyrazin-2-ylamino)-1H-benzimidazol-6-yl]- 2,3-dihydro-1H-isoindol-1-one 389 2-(5-chloro-2-methylphenyl)-3-hydroxy-3-[2-(pyrazin-2-ylamino)-1H- benzimidazol-6-yl]-2,3-dihydro-1H-isoindol-1-one 390 methyl {6-[2-(2-fluoro-3-methylphenyl)-1-hydroxy-3-oxo-2,3-dihydro-1H- isoindol-1-yl]-1H-benzimidazol-2-yl}carbamate 391 3-hydroxy-2-[3-(methyloxy)phenyl]-3-[2-(pyrazin-2-ylamino)-1H-benzimidazol- 5-yl]-2,3-dihydro-1H-isoindol-1-one 392 methyl {6-[(2-{[(2-thienylmethyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 393 methyl {6-[(2-{[(3-methylphenyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 394 methyl {6-[(2-{[(3-bromophenyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 395 methyl {6-[(2-{[(3-chlorophenyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 396 methyl {6-[(2-{[(3-fluorophenyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 397 methyl (6-{[2-({[3-(methyloxy)phenyl]amino}carbonyl)phenyl]carbonyl}-1H- benzimidazol-2-yl)carbamate 398 methyl (6-{[2-({[3-(trifluoromethyl)phenyl]amino}carbonyl)phenyl]carbonyl}- 1H-benzimidazol-2-yl)carbamate 399 methyl {6-[(2-{[(3-ethylphenyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 400 methyl {6-[(2-{[(3-ethynylphenyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 401 methyl {6-[(2-{[(3-chloro-4-fluorophenyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 402 methyl {6-[(2-{[(5-chloro-2-fluorophenyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 403 methyl {6-[(2-{[(3-iodophenyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 404 methyl (6-{[2-({[3-(1-methylethyl)phenyl]amino}carbonyl)phenyl]carbonyl}- 1H-benzimidazol-2-yl)carbamate 405 methyl {6-[(2-{[(3-thienylmethyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 406 methyl {6-[(2-{[(3-bromo-4-fluorophenyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 407 methyl {6-[(2-{[(3-chloro-2-fluorophenyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 408 methyl {6-[(2-{[(4-fluoro-3-methylphenyl)amino]carbonyl}phenyl)carbonyl]- 1H-benzimidazol-2-yl}carbamate 409 methyl {6-[(2-{[(5-bromo-2-fluorophenyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 410 methyl {6-[(2-{[(5-bromo-2,4-difluorophenyl)amino]carbonyl}phenyl)carbonyl]- 1H-benzimidazol-2-yl}carbamate 411 methyl {6-[(2-{[(5-chloro-2,4-difluorophenyl)amino]carbonyl}phenyl)carbonyl]- 1H-benzimidazol-2-yl}carbamate 412 methyl {6-[(2-{[(3-bromo-2-fluorophenyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 413 methyl {6-[(2-{[(3-ethenylphenyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 414 methyl {6-[(2-{[(3-ethynyl-2-fluorophenyl)amino]carbonyl}phenyl)carbonyl]- 1H-benzimidazol-2-yl}carbamate 415 methyl {6-[(2-{[(5-chloro-2-methylphenyl)amino]carbonyl}phenyl)carbonyl]- 1H-benzimidazol-2-yl}carbamate 416 methyl {6-[(2-{[(5-bromo-2-methylphenyl)amino]carbonyl}phenyl)carbonyl]- 1H-benzimidazol-2-yl}carbamate 417 methyl {6-[(2-{[(2-fluoro-3-iodophenyl)amino]carbonyl}phenyl)carbonyl]-1H- benzimidazol-2-yl}carbamate 418 methyl {6-[(2-{[(3-ethenyl-2-fluorophenyl)amino]carbonyl}phenyl)carbonyl]- 1H-benzimidazol-2-yl}carbamate 419 methyl {6-[(2-{[(2-fluoro-5-methylphenyl)amino]carbonyl}phenyl)carbonyl]- 1H-benzimidazol-2-yl}carbamate

Table 7 Representative EGFR and/or VEGFR Inhibitors

The Compounds in Table 7 can be prepared as pharmaceutically acceptable salts, solvates, hydrates, and/or isomers thereof. All such salt, solvate, hydrate, and isomer combinations of the Compounds in Table 7 can be used to practice the invention.

Entry Name 1 (3Z)-3-[[5-(methyloxy)-1H-benzimidazol-2-yl](phenyl)methylidene]-5-{[1- (phenylmethyl)pyrrolidin-3-yl]amino}-1,3-dihydro-2H-indol-2-one 2 (3Z)-5-[(1-ethylpiperidin-3-yl)amino]-3-[[5-(methyloxy)-1H-benzimidazol-2- yl](phenyl)methylidene]-1,3-dihydro-2H-indol-2-one 3 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[[5-(methyloxy)-1H-benzimidazol-2- yl](phenyl)methylidene]-1,3-dihydro-2H-indol-2-one 4 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[1H-imidazol-2-yl(phenyl)methylidene]-1,3- dihydro-2H-indol-2-one 5 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-{[5-(methyloxy)-1H-benzimidazol-2-yl][4- (methyloxy)phenyl]methylidene}-1,3-dihydro-2H-indol-2-one 6 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[[5-(methyloxy)-1H-benzimidazol-2-yl](4- methylphenyl)methylidene]-1,3-dihydro-2H-indol-2-one 7 (3Z)-3-[1H-benzimidazol-2-yl(4-nitrophenyl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 8 (3Z)-3-{1H-benzimidazol-2-yl[4-(methyloxy)phenyl]methylidene}-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 9 (3Z)-3-[1H-benzimidazol-2-yl(phenyl)methylidene]-5-[(1-ethylpiperidin-4-yl)amino]- 1,3-dihydro-2H-indol-2-one 10 (3Z)-3-[[5-(methyloxy)-1H-benzimidazol-2-yl](phenyl)methylidene]-5-[(2,2,6,6- tetramethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 11 (3Z)-3-[(4-aminophenyl)(1H-benzimidazol-2-yl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 12 (3Z)-3-[1H-benzimidazol-2-yl(4-methylphenyl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 13 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[1H-imidazol-2-yl(4- methylphenyl)methylidene]-1,3-dihydro-2H-indol-2-one 14 (3Z)-5-[(1-ethylpiperidin-4-yl)oxy]-3-[[5-(methyloxy)-1H-benzimidazol-2- yl](phenyl)methylidene]-1,3-dihydro-2H-indol-2-one 15 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-{1H-imidazol-2-yl[4- (methyloxy)phenyl]methylidene}-1,3-dihydro-2H-indol-2-one 16 (3Z)-3-[1H-benzimidazol-2-yl(4-fluorophenyl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 17 (3Z)-3-[1H-benzimidazol-2-yl(3,5-difluorophenyl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 18 (3Z)-3-[1H-benzimidazol-2-yl(3-fluorophenyl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 19 (3Z)-3-[1H-benzimidazol-2-yl(3-nitrophenyl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 20 3-((Z)-1H-benzimidazol-2-yl{5-[(1-ethylpiperidin-4-yl)amino]-2-oxo-1,2-dihydro-3H- indol-3-ylidene}methyl)benzonitrile 21 (3Z)-3-[(3-aminophenyl)(1H-benzimidazol-2-yl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 22 (3Z)-3-[1H-benzimidazol-2-yl(phenyl)methylidene]-5-(piperidin-4-ylamino)-1,3- dihydro-2H-indol-2-one 23 3-((Z)-1H-benzimidazol-2-yl{5-[(1-ethylpiperidin-4-yl)amino]-2-oxo-1,2-dihydro-3H- indol-3-ylidene}methyl)benzenecarboximidamide 24 (3Z)-3-[1H-benzimidazol-2-yl(phenyl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 25 (3Z)-3-[1H-benzimidazol-2-yl(phenyl)methylidene]-5-[(2,2,6,6-tetramethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 26 (3Z)-3-{1H-benzimidazol-2-yl[3-(methyloxy)phenyl]methylidene}-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 27 (3Z)-3-[1H-benzimidazol-2-yl(3-chlorophenyl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 28 2-(2-{2-[(Z)-{5-[(1-ethylpiperidin-4-yl)amino]-2-oxo-1,2-dihydro-3H-indol-3- ylidene}(phenyl)methyl]-1H-imidazol-4-yl}ethyl)-1H-isoindole-1,3(2H)-dione 29 (3Z)-3-[1H-benzimidazol-2-yl(phenyl)methylidene]-5-({1-[2- (dimethylamino)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 30 (3Z)-3-[1H-benzimidazol-2-yl(phenyl)methylidene]-5-{[1-(methylsulfonyl)piperidin- 4-yl]amino}-1,3-dihydro-2H-indol-2-one 31 (3Z)-5-(8-azabicyclo[3.2.1]oct-3-ylamino)-3-[1H-benzimidazol-2- yl(phenyl)methylidene]-1,3-dihydro-2H-indol-2-one 32 (3Z)-3-{1H-benzimidazol-2-yl[3-(methyloxy)phenyl]methylidene}-5-[(1- ethylpiperidin-4-yl)oxy]-1,3-dihydro-2H-indol-2-one 33 (3Z)-3-[1H-benzimidazol-2-yl(3,5-difluorophenyl)methylidene]-5-[(1-ethylpiperidin-4- yl)oxy]-1,3-dihydro-2H-indol-2-one 34 (3Z)-3-[1H-benzimidazol-2-yl(phenyl)methylidene]-5-{[1-(phenylmethyl)piperidin-4- yl]oxy}-1,3-dihydro-2H-indol-2-one 35 (3Z)-3-[1H-benzimidazol-2-yl(3-chlorophenyl)methylidene]-5-[(1-ethylpiperidin-4- yl)oxy]-1,3-dihydro-2H-indol-2-one 36 (3Z)-3-[1H-benzimidazol-2-yl(3,5-difluorophenyl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}oxy)-1,3-dihydro-2H-indol-2-one 37 (3Z)-3-[1H-benzimidazol-2-yl(3-chlorophenyl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}oxy)-1,3-dihydro-2H-indol-2-one 38 (3Z)-3-[1H-benzimidazol-2-yl(3-chlorophenyl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 39 (3Z)-3-{1H-benzimidazol-2-yl[3-(methyloxy)phenyl]methylidene}-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 40 (3Z)-3-[(3-chlorophenyl)(1H-imidazol-2-yl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 41 (3Z)-3-[(3-fluorophenyl)(1H-imidazol-2-yl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 42 (3Z)-3-[1H-benzimidazol-2-yl(3,5-difluorophenyl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 43 (3Z)-3-[1H-benzimidazol-2-yl(3-chlorophenyl)methylidene]-5-[(1-ethylpiperidin-4- yl)(methyl)amino]-1,3-dihydro-2H-indol-2-one 44 (3Z)-3-[(3-chlorophenyl)(1H-imidazol-2-yl)methylidene]-5-[(1-ethylpiperidin-4- yl)oxy]-1,3-dihydro-2H-indol-2-one 45 (3Z)-3-[1H-benzimidazol-2-yl(4-chlorophenyl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 46 (3Z)-3-[1H-benzimidazol-2-yl(3-fluorophenyl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 47 (3Z)-3-[1H-benzimidazol-2-yl(4-fluorophenyl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 48 (3Z)-3-[(3-chlorophenyl)(1H-imidazol-2-yl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 49 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[(3-fluorophenyl)(1H-imidazol-2- yl)methylidene]-1,3-dihydro-2H-indol-2-one 50 (3Z)-3-[1H-benzimidazol-2-yl(3-fluoro-4-methylphenyl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 51 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[(3-fluorophenyl)(4-methyl-lH-imidazol-2- yl)methylidene]-1,3-dihydro-2H-indol-2-one 52 (3Z)-3-[1H-benzimidazol-2-yl(4-fluoro-3-methylphenyl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 53 (3Z)-3-[(3-chloro-4-fluorophenyl)(1H-imidazol-2-yl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 54 (3Z)-3-[(3,4-difluorophenyl)(1H-imidazol-2-yl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 55 (3Z)-3-[(5-chloro-1H-benzimidazol-2-yl)(phenyl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 56 (3Z)-3-[(5-chloro-1H-benzimidazol-2-yl)(3,5-difluorophenyl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 57 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[(3-fluoro-4-methylphenyl)(1H-imidazol-2- yl)methylidene]-1,3-dihydro-2H-indol-2-one 58 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[(4-fluorophenyl)(1H-imidazol-2- yl)methylidene]-1,3-dihydro-2H-indol-2-one 59 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[1H-imidazol-2-yl(4- propylphenyl)methylidene]-1,3-dihydro-2H-indol-2-one 60 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-{1H-imidazol-2-yl[4- (trifluoromethyl)phenyl]methylidene}-1,3-dihydro-2H-indol-2-one 61 (3E)-3-[(3,5-difluorophenyl)(5-fluoro-1H-benzimidazol-2-yl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 62 (3Z)-3-[(3,5-difluorophenyl)(5-fluoro-1H-benzimidazol-2-yl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 63 (3Z)-3-[(3-fluoro-4-methylphenyl)(1H-imidazol-2-yl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 64 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[(4-methyl-1H-imidazol-2-yl)(4- methylphenyl)methylidene]-1,3-dihydro-2H-indol-2-one 65 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[[3-fluoro-4-(trifluoromethyl)phenyl](1H- imidazol-2-yl)methylidene]-1,3-dihydro-2H-indol-2-one 66 (3Z)-3-[(4-chlorophenyl)(1H-imidazol-2-yl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 67 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[(3-fluoro-4-methylphenyl)(4-methyl-1H- imidazol-2-yl)methylidene]-1,3-dihydro-2H-indol-2-one 68 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-{1H-imidazol-2-yl[6-(trifluoromethyl)pyridin- 3-yl]methylidene}-1,3-dihydro-2H-indol-2-one 69 (3Z)-3-[1H-imidazol-2-yl(4-methylphenyl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 70 (3Z)-3-[(3-fluorophenyl)(4-methyl-1H-imidazol-2-yl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 71 (3Z)-3-{1H-imidazol-2-yl[4-(trifluoromethyl)phenyl]methylidene}-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 72 (3Z)-3-[(5-chloro-1H-benzimidazol-2-yl)(phenyl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 73 (3Z)-3-[(3,5-difluorophenyl)(1H-imidazol-2-yl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 74 (3Z)-3-[(3,5-difluorophenyl)(4-methyl-1H-imidazol-2-yl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 75 (3Z)-3-[(3,5-difluorophenyl)(1H-imidazol-2-yl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 76 (3Z)-3-[(3,5-difluorophenyl)(4-methyl-1H-imidazol-2-yl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 77 (3Z)-3-[(4-methyl-1H-imidazol-2-yl)(4-methylphenyl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 78 (3Z)-3-[(4-fluorophenyl)(1H-imidazol-2-yl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 79 (3Z)-3-[(3,4-difluorophenyl)(1H-imidazol-2-yl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 80 (3Z)-3-[(3-chloro-4-fluorophenyl)(1H-imidazol-2-yl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 81 (3Z)-3-[(3-fluorophenyl)(1H-imidazol-2-yl)methylidene]-5-(piperidin-4-ylamino)-1,3- dihydro-2H-indol-2-one 82 (3Z)-3-[(3-fluorophenyl)(1H-imidazol-2-yl)methylidene]-5-{[1-(2-piperidin-1- ylethyl)piperidin-4-yl]amino}-1,3-dihydro-2H-indol-2-one 83 (3Z)-3-[(3-fluorophenyl)(1H-imidazol-2-yl)methylidene]-5-{[1-(2-morpholin-4- ylethyl)piperidin-4-yl]amino}-1,3-dihydro-2H-indol-2-one 84 (3Z)-5-({1-[2-(diethylamino)ethyl]piperidin-4-yl}amino)-3-[(3-fluorophenyl)(1H- imidazol-2-yl)methylidene]-1,3-dihydro-2H-indol-2-one 85 (3Z)-3-[(3-fluorophenyl)(1H-imidazol-2-yl)methylidene]-5-{[1-(2-pyrrolidin-1- ylethyl)piperidin-4-yl]amino}-1,3-dihydro-2H-indol-2-one 86 (3Z)-3-[1H-imidazol-2-yl(4-methylphenyl)methylidene]-5-[(1-methylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 87 (3Z)-3-[(3-fluorophenyl)(1H-1,2,4-triazol-5-yl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 88 ethyl 2-{(Z)-(3-fluorophenyl)[5-({1-[2-(methyloxy)ethyl]piperidin-4-yl}amino)-2-oxo- 1,2-dihydro-3H-indol-3-ylidene]methyl}-4-methyl-1H-imidazole-5-carboxylate 89 (3Z)-3-[1H-imidazol-2-yl(phenyl)methylidene]-5-({1-[2-(methyloxy)ethyl]piperidin-4- yl}amino)-1,3-dihydro-2H-indol-2-one 90 (3Z)-3-{1H-imidazol-2-yl[4-(methyloxy)phenyl]methylidene}-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 91 (3Z)-3-[(4-chlorophenyl)(1H-imidazol-2-yl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 92 (3Z)-3-[[3-fluoro-4-(trifluoromethyl)phenyl](1H-imidazol-2-yl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 93 (3Z)-3-[(3-fluorophenyl)(1H-imidazol-2-yl)methylidene]-5-{[1- (methylsulfonyl)piperidin-4-yl]amino}-1,3-dihydro-2H-indol-2-one 94 (3Z)-3-[1H-imidazol-2-yl(4-propylphenyl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 95 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[(3-fluorophenyl)(4-phenyl-1H-imidazol-2- yl)methylidene]-1,3-dihydro-2H-indol-2-one 96 (3Z)-3-[(3-fluorophenyl)(4-phenyl-1H-imidazol-2-yl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 97 (3Z)-3-[(3-fluoro-4-methylphenyl)(4-methyl-1H-imidazol-2-yl)methylidene]-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 98 (3Z)-3-{1H-imidazol-2-yl[6-(trifluoromethyl)pyridin-3-yl]methylidene}-5-({1-[2- (methyloxy)ethyl]piperidin-4-yl}amino)-1,3-dihydro-2H-indol-2-one 99 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[(3-fluorophenyl)(1H-1,2,4-triazol-5- yl)methylidene]-1,3-dihydro-2H-indol-2-one 100 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[[2-fluoro-4-(trifluoromethyl)phenyl](1H- imidazol-2-yl)methylidene]-1,3-dihydro-2H-indol-2-one 101 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-{(4-methyl-1H-imidazol-2-yl)[4- (trifluoromethyl)phenyl]methylidene}-1,3-dihydro-2H-indol-2-one 102 (3Z)-3-[(4-chlorophenyl)(4-methyl-1H-imidazol-2-yl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 103 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[[3-fluoro-4-(trifluoromethyl)phenyl](4- methyl-1H-imidazol-2-yl)methylidene]-1,3-dihydro-2H-indol-2-one 104 (3Z)-3-[(3,4-difluorophenyl)(4-methyl-1H-imidazol-2-yl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 105 (3Z)-3-[(3-chloro-4-fluorophenyl)(4-methyl-1H-imidazol-2-yl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 106 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[(4-fluorophenyl)(4-methyl-1H-imidazol-2- yl)methylidene]-1,3-dihydro-2H-indol-2-one 107 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[(2-fluorophenyl)(1H-imidazol-2- yl)methylidene]-1,3-dihydro-2H-indol-2-one 108 (3Z)-5-[(1-ethylpiperidin-4-yl)amino]-3-[[2-fluoro-4-(trifluoromethyl)phenyl](4- methyl-1H-imidazol-2-yl)methylidene]-1,3-dihydro-2H-indol-2-one 109 (3Z)-3-[(2,3-difluorophenyl)(1H-imidazol-2-yl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 110 (3Z)-3-[(2,3-difluorophenyl)(4-methyl-1H-imidazol-2-yl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 111 (3Z)-3-[(2,4-difluorophenyl)(4-methyl-1H-imidazol-2-yl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 112 (3Z)-3-[(2,4-difluorophenyl)(1H-imidazol-2-yl)methylidene]-5-[(1-ethylpiperidin-4- yl)amino]-1,3-dihydro-2H-indol-2-one 113 (3Z)-3-[(2-fluorophenyl)(4-methyl-1H-imidazol-2-yl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 114 (3Z)-3-[(3-trifluoromethylphenyl)(1H-imidazol-2-yl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 115 (3Z)-3-[(3-trifluoromethylphenyl)(4-methyl-1H-imidazol-2-yl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 116 (3Z)-3-[(2,4-dichloro-5-fluorophenyl)(1H-imidazol-2-yl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 117 (3Z)-3-[(2,4-dichloro-5-fluorophenyl)(4-methyl-1H-imidazol-2-yl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one 118 (3Z)-3-[(4-chloro-2-fluorophenyl)(4-methyl-1H-imidazol-2-yl)methylidene]-5-[(1- ethylpiperidin-4-yl)amino]-1,3-dihydro-2H-indol-2-one

Table 8. c-KIT Inhibitors

The Compounds in Table 8 can be prepared as pharmaceutically acceptable salts, solvates, hydrates, and/or isomers thereof. All such salt, solvate, hydrate, and isomer combinations of the Compounds in Table 8 can be used to practice the invention.

Entry Name 1 N-[5-chloro-2-(methyloxy)phenyl]-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 2 N-phenyl-2-{[3-(1H-tetrazol-1-yl)phenyl]oxy}acetamide 3 N-(2-methylphenyl)-2-{[3-(1H-tetrazol-1-yl)phenyl]oxy}acetamide 4 N-(2-chlorophenyl)-2-{[3-(1H-tetrazol-1-yl)phenyl]oxy}acetamide 5 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 6 ethyl 2-[({[3-(1H-tetrazol-1-yl)phenyl]oxy}acetyl)amino]-4,5,6,7- tetrahydro-1-benzothiophene-3-carboxylate 7 N-(3-chloro-2-methylphenyl)-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 8 N-(3-fluorophenyl)-2-{[3-(1H-tetrazol-1-yl)phenyl]oxy}acetamide 9 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[3-(2H-tetrazol-5- yl)phenyl]oxy}acetamide 10 N-(4-chloro-2-fluorophenyl)-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 11 N-(4-bromo-3-methylphenyl)-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 12 N-(4-morpholin-4-ylphenyl)-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 13 N-[4-fluoro-3-(trifluoromethyl)phenyl]-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 14 N-[4-bromo-3-(trifluoromethyl)phenyl]-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 15 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[4-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 16 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}propanamide 17 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[3-(5-methyl-1H-tetrazol-1- yl)phenyl]oxy}acetamide 18 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[2-methyl-5-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 19 N-(4-chlorophenyl)-N-methyl-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 20 N-[4-chloro-2-(trifluoromethyl)phenyl]-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 21 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[3-(2,5-dioxopyrrolidin-1- yl)phenyl]oxy}acetamide 22 (2E)—N-[4-chloro-3-(trifluoromethyl)phenyl]-3-[3-(1H-tetrazol-1- yl)phenyl]prop-2-enamide 23 N-[4-fluoro-3-(trifluoromethyl)phenyl]-2-{[4-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 24 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[3-(2-methyl-2H-tetrazol-5- yl)phenyl]oxy}acetamide 25 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[2,4-dichloro-5-(1H- tetrazol-1-yl)phenyl]oxy}acetamide 26 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[3-(1H-tetrazol-1- yl)phenyl]thio}acetamide 27 N-[4-chloro-3-(trifluoromethyl)phenyl]-N~2~-[3-(1H-tetrazol-1- yl)phenyl]glycinamide 28 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[2-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 29 methyl 1-{3-[(2-{[4-chloro-3-(trifluoromethyl)phenyl]amino}-2- oxoethyl)oxy]phenyl}-1H-1,2,3-triazole-4-carboxylate 30 1,1-dimethylethyl {4-[({[3-(1H-tetrazol-1- yl)phenyl]oxy}acetyl)amino]phenyl}carbamate 31 1,1-dimethylethyl {4-[({[4-(1H-tetrazol-1- yl)phenyl]oxy}acetyl)amino]phenyl}carbamate 32 N-{4-[(1-ethylpiperidin-4-yl)amino]phenyl}-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 33 N-{4-[(1-ethylpiperidin-3-yl)amino]phenyl}-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 34 N-(4-aminophenyl)-2-{[4-(1H-tetrazol-1-yl)phenyl]oxy}acetamide 35 N-{4-[(1-ethylpiperidin-4-yl)amino]phenyl}-2-{[4-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 36 N-{4-[(1-ethylpiperidin-3-yl)amino]phenyl}-2-{[4-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 37 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-[(3-pyridin-4- ylphenyl)oxy]acetamide 38 N-[4-chloro-3-(trifluoromethyl)phenyl]-N~2~-methyl-N~2~-[3-(1H- tetrazol-1-yl)phenyl]glycinamide 39 N-1,3-benzothiazol-2-yl-2-{[3-(1H-tetrazol-1-yl)phenyl]oxy}acetamide 40 N-quinolin-8-yl-2-{[3-(1H-tetrazol-1-yl)phenyl]oxy}acetamide 41 N-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 42 N-isoquinolin-5-yl-2-{[3-(1H-tetrazol-1-yl)phenyl]oxy}acetamide 43 N-{3-[(phenylmethyl)oxy]phenyl}-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 44 N-[5-methyl-2-(methyloxy)phenyl]-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 45 N-[2,5-bis(methyloxy)phenyl]-2-{[3-(1H-tetrazol-1-yl)phenyl]oxy}acetamide 46 N-(6-fluoro-1,3-benzothiazol-2-yl)-2-{[3-(1H-tetrazol-1-yl)phenyl]oxy}acetamide 47 methyl 3-[({[3-(1H-tetrazol-1-yl)phenyl]oxy}acetyl)amino]benzoate 48 5-chloro-2-[({[3-(1H-tetrazol-1- yl)phenyl]oxy}acetyl)amino]benzamide 49 N-[5-chloro-2,4-bis(methyloxy)phenyl]-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 50 N-[2-(phenyloxy)phenyl]-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 51 N-[3-(aminosulfonyl)phenyl]-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 52 N-[2-(methyloxy)-5-(trifluoromethyl)phenyl]-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 53 N-(4-{[(4-methylphenyl)sulfonyl]amino}phenyl)-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 54 N-(5-phenyl-1H-pyrazol-3-yl)-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 55 N-1,3-benzothiazol-2-yl-2-{[4-(1H-tetrazol-1-yl)phenyl]oxy}acetamide 56 N-quinolin-8-yl-2-{[4-(1H-tetrazol-1-yl)phenyl]oxy}acetamide 57 1,1-dimethylethyl 2-{3-[(2-{[4-chloro-3- (trifluoromethyl)phenyl]amino}-2-oxoethyl)oxy]phenyl}-1H-pyrrole- 1-carboxylate 58 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[3-(1H-pyrrol-2- yl)phenyl]oxy}acetamide 59 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-[(3-pyrimidin-5- ylphenyl)oxy]acetamide 60 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[3-(1H-1,2,3-triazol-1- yl)phenyl]oxy}acetamide 61 4-chloro-N-(2-{[3-(1H-tetrazol-1-yl)phenyl]oxy}ethyl)-3- (trifluoromethyl)aniline 62 N-[4-chloro-3-(trifluoromethyl)phenyl]-N-(2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}ethyl)formamide 63 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-[(3-pyridin-3- ylphenyl)oxy]acetamide 64 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-[(3-furan-3- ylphenyl)oxy]acetamide 65 (2E)—N-[4-fluoro-3-(trifluoromethyl)phenyl]-3-[3-(1H-tetrazol-1- yl)phenyl]prop-2-enamide 66 N-[4-fluoro-3-(trifluoromethyl)phenyl]-3-[3-(1H-tetrazol-1- yl)phenyl]propanamide 67 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[6-(1H-tetrazol-1- yl)pyrimidin-4-yl]oxy}acetamide 68 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[3-(3,5-dimethylisoxazol-4- yl)phenyl]oxy}acetamide 69 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-[(3-quinolin-7- ylphenyl)oxy]acetamide 70 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-[(3-furan-2- ylphenyl)oxy]acetamide 71 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-[3-(1H-tetrazol-1- yl)phenyl]hydrazinecarboxamide 72 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-[(3-dibenzo[b,d]furan-4- ylphenyl)oxy]acetamide 73 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-[(4-pyrimidin-5- ylphenyl)oxy]acetamide 74 N-methyl-N-[4-(methyloxy)phenyl]-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 75 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-{[3-(1H-tetrazol-1- yl)phenyl]methyl}urea 76 N-[4-chloro-3-(trifluoromethyl)phenyl]-N-methyl-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 77 N-[4-fluoro-3-(trifluoromethyl)phenyl]-N~2~-[3-(1H-tetrazol-1- yl)phenyl]glycinamide 78 N-[4-fluoro-3-(trifluoromethyl)phenyl]-2-{[3-(pyridin-2- ylamino)phenyl]oxy}acetamide 79 N-[2-fluoro-5-(trifluoromethyl)phenyl]-2-[3-(1H-tetrazol-1- yl)phenyl]hydrazinecarboxamide 80 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-[(4-pyridin-3- ylphenyl)oxy]acetamide 81 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-[(3-pyrimidin-5- ylphenyl)methyl]urea 82 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-[(4-pyrimidin-5- ylphenyl)methyl]urea 83 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-[(4-pyridin-3- ylphenyl)methyl]urea 84 [3-(1H-tetrazol-1-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 85 N-[4-fluoro-3-(trifluoromethyl)phenyl]-2-[(4-pyrimidin-5- ylphenyl)oxy]acetamide 86 N~2~-[4-chloro-3-(trifluoromethyl)phenyl]-N-[3-(1H-tetrazol-1- yl)phenyl]glycinamide 87 2-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}-N-[3-(1H-tetrazol-1- yl)phenyl]acetamide 88 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[3-methyl-4-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 89 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[4-(1H-1,2,3-triazol-1- yl)phenyl]oxy}acetamide 90 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[3-fluoro-4-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 91 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[2-fluoro-4-(1H-tetrazol-1- yl)phenyl]oxy}acetamide 92 N-({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)-3-(1H- tetrazol-1-yl)benzenesulfonamide 93 N-({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)-N-methyl-3- (1H-tetrazol-1-yl)benzenesulfonamide 94 N-[4-fluoro-3-(trifluoromethyl)phenyl]-2-[(4-pyridin-3- ylphenyl)oxy]acetamide 95 2-({4-[2,4-bis(methyloxy)pyrimidin-5-yl]phenyl}oxy)-N-[4-fluoro-3- (trifluoromethyl)phenyl]acetamide 96 2-({4-[2,4-bis(methyloxy)pyrimidin-5-yl]phenyl}oxy)-N-[4-chloro-3- (trifluoromethyl)phenyl]acetamide 97 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-[(4-pyridin-4- ylphenyl)oxy]acetamide 98 N-[4-chloro-3-(trifluoromethyl)phenyl]-N~2~-[3-(methyloxy)-4-(1H- tetrazol-1-yl)phenyl]glycinamide 99 N-[4-chloro-3-(trifluoromethyl)phenyl]-N~2~-[4-(methyloxy)-3-(1H- tetrazol-1-yl)phenyl]glycinamide 100 N-[4-chloro-3-(trifluoromethyl)phenyl]-N~2~-[4-(1H-tetrazol-1- yl)phenyl]glycinamide 101 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-(2,3,5,6-tetrafluoro-4- pyrimidin-5-ylphenyl)hydrazinecarboxamide 102 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-{[4-(1H-tetrazol-1- yl)phenyl]methyl}urea 103 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-(4-pyrimidin-5- ylphenyl)hydrazinecarboxamide 104 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-[(3-pyridin-3- ylphenyl)methyl]urea 105 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-methyl-2-{[3-(1H-tetrazol-1- yl)phenyl]oxy}propanamide 106 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[4-(1H-tetrazol-1- yl)phenyl]oxy}propanamide 107 N-({4-[2,4-bis(methyloxy)pyrimidin-5-yl]phenyl}methyl)-N′-[4- chloro-3-(trifluoromethyl)phenyl]urea 108 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-({3-[2- (methyloxy)pyrimidin-5-yl]phenyl}methyl)urea 109 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-({3-[6-(methyloxy)pyridin- 3-yl]phenyl}methyl)urea 110 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-({4-[2- (methyloxy)pyrimidin-5-yl]phenyl}methyl)urea 111 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-({4-[6-(methyloxy)pyridin- 3-yl]phenyl}methyl)urea 112 1,1-dimethylethyl 2-{4-[(2-{[4-chloro-3- (trifluoromethyl)phenyl]amino}-2-oxoethyl)oxy]phenyl}-1H-indole-1- carboxylate 113 N-({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)-4-(1H- tetrazol-1-yl)benzenesulfonamide 114 N-[4-chloro-3-(trifluoromethyl)phenyl]-N~2~-[3-(2H-tetrazol-5- yl)phenyl]glycinamide 115 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[2,6-difluoro-4-(1H- tetrazol-1-yl)phenyl]oxy}acetamide 116 (3-pyridin-3-ylphenyl)methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 117 (3-pyrimidin-5-ylphenyl)methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 118 (3-pyridin-4-ylphenyl)methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 119 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-[4-(1H-tetrazol-1- yl)phenyl]hydrazinecarboxamide 120 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-(4-pyridin-3- ylphenyl)hydrazinecarboxamide 121 (4-pyridin-3-ylphenyl)methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 122 (4-pyridin-4-ylphenyl)methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 123 (4-pyrimidin-5-ylphenyl)methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 124 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-[(4-pyridin-4- ylphenyl)methyl]urea 125 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-(3-pyridin-3- ylphenyl)hydrazinecarboxamide 126 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-(3-pyrimidin-5- ylphenyl)hydrazinecarboxamide 127 N-[5-chloro-2,4-bis(methyloxy)phenyl]-N′-[(4-pyrimidin-5- ylphenyl)methyl]urea 128 N-[5-chloro-2,4-bis(methyloxy)phenyl]-N′-[(4-pyridin-3- ylphenyl)methyl]urea 129 (4-pyrimidin-5-ylphenyl)methyl [5-chloro-2,4- bis(methyloxy)phenyl]carbamate 130 (4-pyridin-3-ylphenyl)methyl [5-chloro-2,4- bis(methyloxy)phenyl]carbamate 131 1-(4-pyridin-3-ylphenyl)ethyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 132 1-(4-pyrimidin-5-ylphenyl)ethyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 133 N-[5-chloro-2,4-bis(methyloxy)phenyl]-N′-[(3-pyridin-3- ylphenyl)methyl]urea 134 N-[5-chloro-2,4-bis(methyloxy)phenyl]-N′-[(3-pyrimidin-5- ylphenyl)methyl]urea 135 (3-pyridin-3-ylphenyl)methyl [5-chloro-2,4-bis(methyloxy)phenyl]carbamate 136 (3-pyrimidin-5-ylphenyl)methyl [5-chloro-2,4-bis(methyloxy)phenyl]carbamate 137 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-methyl-2-(3-pyrimidin-5- ylphenyl)hydrazinecarboxamide 138 N-[4-fluoro-3-(trifluoromethyl)phenyl]-N′-[(4-pyridin-3- ylphenyl)methyl]urea 139 N-{[3-(6-aminopyridin-3-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 140 N-{[4-(6-aminopyridin-3-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 141 N-{[3-(2-aminopyrimidin-5-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 142 N-{[4-(2-aminopyrimidin-5-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 143 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-[1-(4-pyridin-3- ylphenyl)ethyl]urea 144 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-[1-(4-pyrimidin-5- ylphenyl)ethyl]urea 145 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[4-(1H-indol-2- yl)phenyl]oxy}acetamide 146 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-(isoquinolin-7-yloxy)acetamide 147 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-(4-pyridin-4- ylphenyl)hydrazinecarboxamide 148 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-(3-pyridin-4- ylphenyl)hydrazinecarboxamide 149 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-[(3-pyridin-4-ylphenyl)methyl]urea 150 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-[(3-quinoxalin-6- ylphenyl)methyl]urea 151 methyl 3-amino-6-(3-{[({[4-chloro-3- (trifluoromethyl)phenyl]amino}carbonyl)amino]methyl}phenyl)pyrazine- 2-carboxylate 152 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-[(4-quinoxalin-6- ylphenyl)methyl]urea 153 N-{[3-(2-amino-5-methylpyridin-3-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 154 methyl 3-amino-6-(4-{[({[4-chloro-3- (trifluoromethyl)phenyl]amino}carbonyl)amino]methyl}phenyl)pyrazine- 2-carboxylate 155 [3-(1H-tetrazol-1-yl)phenyl]methyl [3-chloro-4- (methyloxy)phenyl]carbamate 156 N-[3-chloro-4-(methyloxy)phenyl]-N′-{[3-(1H-tetrazol-1- yl)phenyl]methyl}urea 157 N-[4-chloro-3-(trifluoromethyl)phenyl]-2-{[4-(5-hydroxy-1H-tetrazol- 1-yl)phenyl]oxy}acetamide 158 N-{[3-(2-amino-5-chloropyridin-3-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 159 N-{[4-(2-amino-5-chloropyridin-3-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 160 N-{[3-(6-chloropyridin-3-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 161 N-{[4-(6-chloropyridin-3-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 162 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-{[4-(pyrimidin-2- yloxy)phenyl]methyl}urea 163 N-({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)-3-(1H- tetrazol-1-yl)benzamide 164 3-amino-6-(3-{[({[4-chloro-3- (trifluoromethyl)phenyl]amino}carbonyl)amino]methyl}phenyl)-N-[2- (dimethylamino)ethyl]pyrazine-2-carboxamide 165 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-{[3-(6-fluoropyridin-3- yl)phenyl]methyl}urea 166 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-({3-[2-(methyloxy)pyridin- 3-yl]phenyl}methyl)urea 167 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-{[4-(6-fluoropyridin-3- yl)phenyl]methyl}urea 168 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-({4-[2-(methyloxy)pyridin- 3-yl]phenyl}methyl)urea 169 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-{[4-(6-methylpyridin-3- yl)phenyl]methyl}urea 170 N-{[4-(2-amino-5-fluoropyridin-3-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 171 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-{[3-(6-methylpyridin-3- yl)phenyl]methyl}urea 172 N-{[4-(2-aminopyridin-3-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 173 N-{[3-(2-aminopyridin-3-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 174 [3-(6-methylpyridin-3-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 175 [3-(2-amino-5-fluoropyridin-3-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 176 [3-(2-aminopyridin-3-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 177 (3-pyrazin-2-ylphenyl)methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 178 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-({3-[6- (hydroxymethyl)pyridin-3-yl]phenyl}methyl)urea 179 N-{[3-(6-acetylpyridin-3-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 180 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-{[3-(6-cyanopyridin-3- yl)phenyl]methyl}urea 181 1,1-dimethylethyl (3S)-3-({[3-amino-6-(3-{[({[4-chloro-3- (trifluoromethyl)phenyl]amino}carbonyl)amino]methyl}phenyl)pyrazin- 2-yl]carbonyl}amino)piperidine-1-carboxylate 182 3-amino-6-(3-{[({[4-chloro-3- (trifluoromethyl)phenyl]amino}carbonyl)amino]methyl}phenyl)-N- [(3S)-piperidin-3-yl]pyrazine-2-carboxamide 183 1,1-dimethylethyl (3S)-3-({[3-amino-6-(4-{[({[4-chloro-3- (trifluoromethyl)phenyl]amino}carbonyl)amino]methyl}phenyl)pyrazin- 2-yl]carbonyl}amino)piperidine-1-carboxylate 184 3-amino-6-(4-{[({[4-chloro-3- (trifluoromethyl)phenyl]amino}carbonyl)amino]methyl}phenyl)-N- [(3S)-piperidin-3-yl]pyrazine-2-carboxamide 185 [3-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 186 N-{[3-(2-amino-5-fluoropyridin-3-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 187 [6-(1H-tetrazol-1-yl)pyridin-2-yl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 188 [3-(1H-benzimidazol-2-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 189 [3-(6-amino-2-methylpyridin-3-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 190 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-({3-[5-(methylthio)pyridin- 3-yl]phenyl}methyl)urea 191 [4-(6-methylpyridin-3-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 192 [4-(2-amino-5-fluoropyridin-3-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 193 [4-(2-aminopyridin-3-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 194 (4-pyrazin-2-ylphenyl)methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 195 [4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 196 [4-(6-amino-2-methylpyridin-3-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 197 [3-(1H-tetrazol-1-yl)phenyl]methyl 1,3-benzothiazol-2-ylcarbamate 198 [3-(1H-tetrazol-1-yl)phenyl]methyl (5-bromopyridin-2-yl)carbamate 199 (3-pyridin-3-ylphenyl)methyl (3,5-dimethylphenyl)carbamate 200 (3-pyridin-3-ylphenyl)methyl [5-chloro-2- (methyloxy)phenyl]carbamate 201 [4-(1H-tetrazol-1-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 202 (3-pyrimidin-5-ylphenyl)methyl [5-chloro-2- (methyloxy)phenyl]carbamate 203 (4-pyrimidin-5-ylphenyl)methyl (3,4-dimethylphenyl)carbamate 204 (3-pyridin-3-ylphenyl)methyl (3,4-dimethylphenyl)carbamate 205 1,1-dimethylethyl 3-({[3-amino-6-(3-{[({[4-chloro-3- (trifluoromethyl)phenyl]amino}carbonyl)amino]methyl}phenyl)pyrazin- 2-yl]carbonyl}amino)piperidine-1-carboxylate 206 1,1-dimethylethyl 3-({[3-amino-6-(4-{[({[4-chloro-3- (trifluoromethyl)phenyl]amino}carbonyl)amino]methyl}phenyl)pyrazin- 2-yl]carbonyl}amino)piperidine-1-carboxylate 207 3-amino-6-(3-{[({[4-chloro-3- (trifluoromethyl)phenyl]amino}carbonyl)amino]methyl}phenyl)-N- piperidin-3-ylpyrazine-2-carboxamide 208 3-amino-6-(4-{[({[4-chloro-3- (trifluoromethyl)phenyl]amino}carbonyl)amino]methyl}phenyl)-N- piperidin-3-ylpyrazine-2-carboxamide 209 1,1-dimethylethyl 4-{[3-amino-6-(3-{[({[4-chloro-3- (trifluoromethyl)phenyl]amino}carbonyl)amino]methyl}phenyl)pyrazin- 2-yl]carbonyl}piperazine-1-carboxylate 210 1,1-dimethylethyl 4-{[3-amino-6-(4-{[({[4-chloro-3- (trifluoromethyl)phenyl]amino}carbonyl)amino]methyl}phenyl)pyrazin- 2-yl]carbonyl}piperazine-1-carboxylate 211 N-({3-[5-amino-6-(piperazin-1-ylcarbonyl)pyrazin-2- yl]phenyl}methyl)-N′-[4-chloro-3-(trifluoromethyl)phenyl]urea 212 N-({4-[5-amino-6-(piperazin-1-ylcarbonyl)pyrazin-2- yl]phenyl}methyl)-N′-[4-chloro-3-(trifluoromethyl)phenyl]urea 213 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-{[3-(1H-pyrazol-4- yl)phenyl]methyl}urea 214 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-{[4-(1H-pyrazol-4- yl)phenyl]methyl}urea 215 [3-(2-piperazin-1-ylpyrimidin-5-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 216 [4-(2-piperazin-1-ylpyrimidin-5-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 217 N-{[3-(2-chloropyridin-3-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 218 N-{[4-(2-chloropyridin-3-yl)phenyl]methyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 219 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-{[3-(2-fluoropyridin-3- yl)phenyl]methyl}urea 220 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-{[4-(2-fluoropyridin-3- yl)phenyl]methyl}urea 221 [3-(1H-tetrazol-1-yl)phenyl]methyl [3- (trifluoromethyl)phenyl]carbamate 222 [3-(1H-tetrazol-1-yl)phenyl]methyl [6-(trifluoromethyl)pyridin-2-yl]carbamate 223 [3-(1H-tetrazol-1-yl)phenyl]methyl [4-(trifluoromethyl)pyridin-2-yl]carbamate 224 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-({3-[5-(methylthio)pyridin- 2-yl]phenyl}methyl)urea 225 [3-(2,6-dimethylpyridin-3-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 226 {3-[5-(methyloxy)pyridin-3-yl]phenyl}methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 227 2,3′-bipyridin-6-ylmethyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 228 (6-pyrimidin-5-ylpyridin-2-yl)methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 229 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-[(3-isoquinolin-4- ylphenyl)methyl]urea 230 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-[(4-isoquinolin-4- ylphenyl)methyl]urea 231 [6-(1H-tetrazol-1-yl)pyridin-2-yl]methyl [4-(trifluoromethyl)pyridin-2- yl]carbamate 232 [3-(1H-pyrazol-4-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate 233 [4-(1H-pyrazol-4-yl)phenyl]methyl [4-chloro-3- (trifluoromethyl)phenyl]carbamate

Table 9. c-KIT and/or Flt-3 Inhibitors

The Compounds in Table 9 can be prepared as pharmaceutically acceptable salts, solvates, hydrates, and/or isomers thereof. All such salt, solvate, hydrate, and isomer combinations of the Compounds in Table 9 can be used to practice the invention.

Entry Name 1 4-((E)-2-{3-[6-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]-1H-pyrazol-5- yl}ethenyl)phenol 2 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-(4-{3-[5-(4-ethylpiperazin-1-yl)-1H- benzimidazol-2-yl]-1H-pyrazol-5-yl}phenyl)urea 3 N-(3-ethylphenyl)-N′-(4-{3-[5-(4-ethylpiperazin-1-yl)-1H-benzimidazol-2-yl]-1H- pyrazol-5-yl}phenyl)urea 4 N-(4-{3-[5-(4-ethylpiperazin-1-yl)-1H-benzimidazol-2-yl]-1H-pyrazol-5- yl}phenyl)-N′-[3-(trifluoromethyl)phenyl]urea 5 N-(3-acetylphenyl)-N′-(4-{3-[5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]- 1H-pyrazol-5-yl}phenyl)urea 6 N-(3,4-dichlorophenyl)-N′-(4-{3-[5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2- yl]-1H-pyrazol-5-yl}phenyl)urea 7 N-(3-bromophenyl)-N′-(4-{3-[6-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]- 1H-pyrazol-5-yl}phenyl)urea 8 N-[4-fluoro-3-(trifluoromethyl)phenyl]-N′-(4-{3-[5-(4-methylpiperazin-1-yl)-1H- benzimidazol-2-yl]-1H-pyrazol-5-yl}phenyl)urea 9 N-(4-{3-[5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]-1H-pyrazol-5- yl}phenyl)-N′-[4-(phenyloxy)phenyl]urea 10 N-(3-chlorophenyl)-N′-(4-{3-[5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]- 1H-pyrazol-5-yl}phenyl)urea 11 N-[3,5-bis(methyloxy)phenyl]-N′-(4-{3-[6-(4-methylpiperazin-1-yl)-1H- benzimidazol-2-yl]-1H-pyrazol-5-yl}phenyl)urea 12 N-(4-{3-[5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]-1H-pyrazol-5- yl}phenyl)-N′-{4-[(trifluoromethyl)oxy]phenyl}urea 13 N-(4-{3-[6-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]-1H-pyrazol-5- yl}phenyl)-N′-[4-(trifluoromethyl)phenyl]urea 14 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-(4-{3-[5-(4-methylpiperazin-1-yl)-1H- benzimidazol-2-yl]-1H-pyrazol-5-yl}phenyl)urea 15 N-(4-{3-[5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]-1H-pyrazol-5- yl}phenyl)-N′-[3-(trifluoromethyl)phenyl]urea 16 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-(4-{3-[4-(4-methylpiperazin-1- yl)phenyl]-1H-pyrazol-5-yl}phenyl)urea 17 N-(3,4-dimethylphenyl)-N′-(4-{5-[4-(4-methylpiperazin-1-yl)phenyl]-1H-pyrazol- 3-yl}phenyl)urea 18 N-(4-chlorophenyl)-N′-(4-{3-[5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]- 1H-pyrazol-5-yl}phenyl)urea 19 N-(3,5-difluorophenyl)-N′-(4-{3-[5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2- yl]-1H-pyrazol-5-yl}phenyl)urea 20 N-[3-(methyloxy)phenyl]-N′-(4-{3-[5-(4-methylpiperazin-1-yl)-1H-benzimidazol- 2-yl]-1H-pyrazol-5-yl}phenyl)urea 21 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-(4-{3-[4-(4-ethylpiperazin-1-yl)phenyl]- 1H-pyrazol-5-yl}phenyl)urea 22 N-(3-fluorophenyl)-N′-(4-{3-[5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]- 1H-pyrazol-5-yl}phenyl)urea 23 N-(4-fluorophenyl)-N′-(4-{3-[5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]- 1H-pyrazol-5-yl}phenyl)urea 24 N-(3-cyanophenyl)-N′-(4-{3-[6-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]- 1H-pyrazol-5-yl}phenyl)urea 25 N-(3,4-difluorophenyl)-N′-(4-{3-[5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2- yl]-1H-pyrazol-5-yl}phenyl)urea 26 N-[3,4-bis(methyloxy)phenyl]-N′-(4-{3-[5-(4-methylpiperazin-1-yl)-1H- benzimidazol-2-yl]-1H-pyrazol-5-yl}phenyl)urea 27 N-[5-chloro-2-(methyloxy)phenyl]-N′-(4-{5-[4-(4-methylpiperazin-1-yl)phenyl]- 1H-pyrazol-3-yl}phenyl)urea 28 N-(4-{5-[4-(4-methylpiperazin-1-yl)phenyl]-1H-pyrazol-3-yl}phenyl)-N′-[4- (phenyloxy)phenyl]urea 29 N-(2,4-difluorophenyl)-N′-(4-{3-[6-(4-ethylpiperazin-1-yl)-1H-benzimidazol-2-yl]- 1H-pyrazol-5-yl}phenyl)urea 30 N-{4-[3-(1H-benzimidazol-2-yl)-1H-pyrazol-5-yl]phenyl}-N′-[4-chloro-3- (trifluoromethyl)phenyl]urea 31 N-{4-[3-(1H-benzimidazol-2-yl)-1H-pyrazol-5-yl]phenyl}-N′-[2-fluoro-5- (trifluoromethyl)phenyl]urea 32 N-(2,4-difluorophenyl)-N′-(4-{3-[5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2- yl]-1H-pyrazol-5-yl}phenyl)urea 33 N-{4-[3-(1H-benzimidazol-2-yl)-1H-pyrazol-5-yl]phenyl}-N′-phenylurea 34 N-[3,5-bis(trifluoromethyl)phenyl]-N′-(4-{3-[5-(4-methylpiperazin-1-yl)-1H- benzimidazol-2-yl]-1H-pyrazol-5-yl}phenyl)urea 35 N-(2-fluorophenyl)-N′-(4-{3-[5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]- 1H-pyrazol-5-yl}phenyl)urea 36 4-((E)-2-{5-[(E)-2-phenylethenyl]-1H-pyrazol-3-yl}ethenyl)phenol 37 2-(methyloxy)-4-((E)-2-{5-[(E)-2-phenylethenyl]-1H-pyrazol-3-yl}ethenyl)phenol 38 N-(5-fluoro-2-methylphenyl)-N′-(4-{3-[6-(4-methylpiperazin-1-yl)-1H- benzimidazol-2-yl]-1H-pyrazol-5-yl}phenyl)urea 39 N-(4-{3-[5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]-1H-pyrazol-5- yl}phenyl)-N′-phenylurea 40 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-(4-{3-[3-(4-methylpiperazin-1- yl)phenyl]-1H-pyrazol-5-yl}phenyl)urea 41 N-(2,4-difluorophenyl)-N′-(4-{3-[4-(4-methylpiperazin-1-yl)phenyl]-1H-pyrazol-5- yl}phenyl)urea 42 N-(2,3-dihydro-1,4-benzodioxin-6-yl)-N′-(4-{5-[4-(4-methylpiperazin-1- yl)phenyl]-1H-pyrazol-3-yl}phenyl)urea 43 N-[2,4-bis(methyloxy)phenyl]-N′-(4-{5-[4-(4-methylpiperazin-1-yl)phenyl]-1H- pyrazol-3-yl}phenyl)urea 44 4-((E)-2-{3-[(E)-2-(4-fluorophenyl)ethenyl]-1H-pyrazol-5-yl}ethenyl)-2- (methyloxy)phenol 45 4-{(E)-2-[3-(1-benzofuran-2-yl)-1H-pyrazol-5-yl]ethenyl}phenol 46 N-(4-{3-[4-(4-methylpiperazin-1-yl)phenyl]-1H-pyrazol-5-yl}phenyl)-N′-(2- phenylethyl)ethanediamide 47 4-{(E)-2-[3-(1H-benzimidazol-2-yl)-1H-pyrazol-5-yl]ethenyl}phenol 48 4-((E)-2-{3-[(E)-2-(4-chlorophenyl)ethenyl]-1H-pyrazol-5-yl}ethenyl)-2- (methyloxy)phenol 49 4-{(E)-2-[3-(1-benzothien-2-yl)-1H-pyrazol-5-yl]ethenyl}phenol 50 N-[4-chloro-3-(trifluoromethyl)phenyl]-N′-[4-(3-phenyl-1H-pyrazol-5- yl)phenyl]urea 51 4-((E)-2-{3-[4-(4-methylpiperazin-1-yl)phenyl]-1H-pyrazol-5-yl}ethenyl)phenol 52 1,1-dimethylethyl {4-[3-(1H-benzimidazol-2-yl)-1H-pyrazol-5- yl]phenyl}carbamate 53 N-(5-fluoro-2-methylphenyl)-N′-(4-{5-[4-(4-methylpiperazin-1-yl)phenyl]-1H- pyrazol-3-yl}phenyl)urea 54 4-[(E)-2-(3-phenyl-1H-pyrazol-5-yl)ethenyl]phenol 55 2-(methyloxy)-4-[(E)-2-(5-phenyl-1H-pyrazol-3-yl)ethenyl]phenol 56 4-[(E)-2-(5-naphthalen-2-yl-1H-pyrazol-3-yl)ethenyl]phenol 57 4-{(E)-2-[5-(2-fluorophenyl)-1H-pyrazol-3-yl]ethenyl}phenol 58 4-((E)-2-{3-[3-(4-methylpiperazin-1-yl)phenyl]-1H-pyrazol-5-yl}ethenyl)phenol 59 4-((E)-2-{3-[(E)-2-(2,4-difluorophenyl)ethenyl]-1H-pyrazol-5-yl}ethenyl)-2- (methyloxy)phenol 60 4-{(E)-2-[5-(4-fluorophenyl)-1H-pyrazol-3-yl]ethenyl}phenol 61 4-{(E)-2-[3-(4-chlorophenyl)-1H-pyrazol-5-yl]ethenyl}phenol 62 4-[(E)-2-(5-pyridin-2-yl-1H-pyrazol-3-yl)ethenyl]phenol 63 4-{(E)-2-[3-(5-chloro-1-benzofuran-2-yl)-1H-pyrazol-5-yl]ethenyl}phenol 64 N-(1,1-dimethylethyl)-N′-(4-{3-[5-(4-ethylpiperazin-1-yl)-1H-benzimidazol-2-yl]- 1H-pyrazol-5-yl}phenyl)urea 65 4-[(E)-2-(3-pyridin-4-yl-1H-pyrazol-5-yl)ethenyl]phenol 66 4-{(E)-2-[3-(3-chlorophenyl)-1H-pyrazol-5-yl]ethenyl}phenol 67 4-((E)-2-{5-[2-(methyloxy)phenyl]-1H-pyrazol-3-yl}ethenyl)phenol 68 4-{(E)-2-[3-(2-chlorophenyl)-1H-pyrazol-5-yl]ethenyl}phenol 69 4-[(E)-2-(3-pyridin-3-yl-1H-pyrazol-5-yl)ethenyl]phenol 70 4-((E)-2-{5-[3-(methyloxy)phenyl]-1H-pyrazol-3-yl}ethenyl)phenol 71 1,1-dimethylethyl (4-{3-[(E)-2-phenylethenyl]-1H-pyrazol-5-yl}phenyl)carbamate 72 4-{(E)-2-[3-(3,4-dichlorophenyl)-1H-pyrazol-5-yl]ethenyl}phenol 73 2-{5-[(E)-2-phenylethenyl]-1H-pyrazol-3-yl}-1-benzofuran-6-ol 74 4-{(E)-2-[5-(3-fluorophenyl)-1H-pyrazol-3-yl]ethenyl}phenol 75 2-(5-phenyl-1H-pyrazol-3-yl)-1H-benzimidazole 76 N-phenyl-N′-[4-(3-phenyl-1H-pyrazol-5-yl)phenyl]urea 77 4-[3-(1H-benzimidazol-2-yl)-1H-pyrazol-5-yl]aniline 78 4-[(E)-2-(5-biphenyl-3-yl-1H-pyrazol-3-yl)ethenyl]phenol 79 4-((E)-2-{5-[5-(4-methylpiperazin-1-yl)-1H- benzimidazol-2-yl]-1H-pyrazol-3-yl}ethenyl)phenol

General Administration

In one aspect, the invention provides pharmaceutical compositions comprising an inhibitor of PI3K according to the invention and a pharmaceutically acceptable carrier, excipient, or diluent. In certain other specific embodiments, administration may specifically be by the oral route. Administration of the compounds of the invention, or their pharmaceutically acceptable salts, in pure form or in an appropriate pharmaceutical composition, can be carried out via any of the accepted modes of administration or agents for serving similar utilities. Thus, administration can be, for example, orally, nasally, parenterally (intravenous, intramuscular, or subcutaneous), topically, transdermally, intravaginally, intravesically, intracistemally, or rectally, in the form of solid, semi-solid, lyophilized powder, or liquid dosage forms, such as for example, tablets, suppositories, pills, soft elastic and hard gelatin capsules, powders, solutions, suspensions, or aerosols, or the like, specifically in unit dosage forms suitable for simple administration of precise dosages. When treating brain cancers, including glioblastomas, the administration may specifically be by placing a gliadel, a dissolvable material that contains the chemotherapy drug (in particular BCNU), directly into brain tumors during an operation.

The compositions will include a compound of Formula I or II as the/an active agent and can include a conventional pharmaceutical carrier or excipient and in addition may include other medicinal agents and pharmaceutical agents that are generally administered to a patient being treated for cancer.

Adjuvants include preserving, wetting, suspending, sweetening, flavoring, perfuming, emulsifying, and dispensing agents. Prevention of the action of microorganisms can be ensured by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, and the like. It may also be desirable to include isotonic agents, for example sugars, sodium chloride, and the like. Prolonged absorption of the injectable pharmaceutical form can be brought about by the use of agents delaying absorption, for example, aluminum monostearate and gelatin.

If desired, a pharmaceutical composition of the invention may also contain minor amounts of auxiliary substances such as wetting or emulsifying agents, pH buffering agents, antioxidants, and the like, such as, for example, citric acid, sorbitan monolaurate, triethanolamine oleate, butylalted hydroxytoluene, etc.

The choice of formulation depends on various factors such as the mode of drug administration (e.g., for oral administration, formulations in the form of tablets, pills or capsules) and the bioavailability of the drug substance. Recently, pharmaceutical formulations have been developed especially for drugs that show poor bioavailability based upon the principle that bioavailability can be increased by increasing the surface area i.e., decreasing particle size. For example, U.S. Pat. No. 4,107,288 describes a pharmaceutical formulation having particles in the size range from 10 to 1,000 nm in which the active material is supported on a crosslinked matrix of macromolecules. U.S. Pat. No. 5,145,684 describes the production of a pharmaceutical formulation in which the drug substance is pulverized to nanoparticles (average particle size of 400 nm) in the presence of a surface modifier and then dispersed in a liquid medium to give a pharmaceutical formulation that exhibits remarkably high bioavailability.

Compositions suitable for parenteral injection may comprise physiologically acceptable sterile aqueous or nonaqueous solutions, dispersions, suspensions or emulsions, and sterile powders for reconstitution into sterile injectable solutions or dispersions. Examples of suitable aqueous and nonaqueous carriers, diluents, solvents or vehicles include water, ethanol, polyols (propyleneglycol, polyethyleneglycol, glycerol, and the like), suitable mixtures thereof, vegetable oils (such as olive oil) and injectable organic esters such as ethyl oleate. Proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersions and by the use of surfactants.

One specific route of administration is oral, using a convenient daily dosage regimen that can be adjusted according to the degree of severity of the disease-state to be treated.

Solid dosage forms for oral administration include capsules, tablets, pills, powders, and granules. In such solid dosage forms, the active compound is admixed with at least one inert customary excipient (or carrier) such as sodium citrate or dicalcium phosphate or (a) fillers or extenders, as for example, starches, lactose, sucrose, glucose, mannitol, and silicic acid, (b) binders, as for example, cellulose derivatives, starch, alignates, gelatin, polyvinylpyrrolidone, sucrose, and gum acacia, (c) humectants, as for example, glycerol, (d) disintegrating agents, as for example, agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, croscarmellose sodium, complex silicates, and sodium carbonate, (e) solution retarders, as for example paraffin, (f) absorption accelerators, as for example, quaternary ammonium compounds, (g) wetting agents, as for example, cetyl alcohol, and glycerol monostearate, magnesium stearate and the like (h) adsorbents, as for example, kaolin and bentonite, and (i) lubricants, as for example, talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, or mixtures thereof. In the case of capsules, tablets, and pills, the dosage forms may also comprise buffering agents.

Solid dosage forms as described above can be prepared with coatings and shells, such as enteric coatings and others well known in the art. They may contain pacifying agents, and can also be of such composition that they release the active compound or compounds in a certain part of the intestinal tract in a delayed manner. Examples of embedded compositions that can be used are polymeric substances and waxes. The active compounds can also be in microencapsulated form, if appropriate, with one or more of the above-mentioned excipients.

Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, solutions, suspensions, syrups, and elixirs. Such dosage forms are prepared, for example, by dissolving, dispersing, etc., a compound(s) of the invention, or a pharmaceutically acceptable salt or solvate thereof, and optional pharmaceutical adjuvants in a carrier, such as, for example, water, saline, aqueous dextrose, glycerol, ethanol and the like; solubilizing agents and emulsifiers, as for example, ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propyleneglycol, 1,3-butyleneglycol, dimethylformamide; oils, in particular, cottonseed oil, groundnut oil, corn germ oil, olive oil, castor oil and sesame oil, glycerol, tetrahydrofurfuryl alcohol, polyethyleneglycols and fatty acid esters of sorbitan; or mixtures of these substances, and the like, to thereby form a solution or suspension.

Suspensions, in addition to the active compounds, may contain suspending agents, as for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar-agar and tragacanth, or mixtures of these substances, and the like.

Compositions for rectal administrations are, for example, suppositories that can be prepared by mixing the compounds of the present invention with for example suitable non-irritating excipients or carriers such as cocoa butter, polyethyleneglycol or a suppository wax, which are solid at ordinary temperatures but liquid at body temperature and therefore, melt while in a suitable body cavity and release the active component therein.

Dosage forms for topical administration of a compound of this invention include ointments, powders, sprays, and inhalants. The active component is admixed under sterile conditions with a physiologically acceptable carrier and any preservatives, buffers, or propellants as may be required. Ophthalmic formulations, eye ointments, powders, and solutions are also contemplated as being within the scope of this invention.

Compressed gases may be used to disperse a compound of this invention in aerosol form. Inert gases suitable for this purpose are nitrogen, carbon dioxide, etc.

Generally, depending on the intended mode of administration, the pharmaceutically acceptable compositions will contain about 1% to about 99% by weight of a compound(s) of the invention, or a pharmaceutically acceptable salt or solvate thereof, and 99% to 1% by weight of a suitable pharmaceutical excipient. In one example, the composition will be between about 5% and about 75% by weight of a compound(s) of the invention, or a pharmaceutically acceptable salt or solvate thereof, with the rest being suitable pharmaceutical excipients.

Actual methods of preparing such dosage forms are known, or will be apparent, to those skilled in this art; for example, see Remington's Pharmaceutical Sciences, 18th Ed., (Mack Publishing Company, Easton, Pa., 1990). The composition to be administered will, in any event, contain a therapeutically effective amount of a compound of the invention, or a pharmaceutically acceptable salt or solvate thereof, for treatment of a disease-state in accordance with the teachings of this invention.

The compounds of the invention, or their pharmaceutically acceptable salts, are administered in a therapeutically effective amount which will vary depending upon a variety of factors including the activity of the specific compound employed, the metabolic stability and length of action of the compound, the age, body weight, general health, sex, diet, mode and time of administration, rate of excretion, drug combination, the severity of the particular disease-states, and the host undergoing therapy. The compounds of the present invention can be administered to a patient at dosage levels in the range of about 0.1 to about 1,000 mg per day. For a normal human adult having a body weight of about 70 kilograms, a dosage in the range of about 0.01 to about 100 mg per kilogram of body weight per day is an example. The specific dosage used, however, can vary. For example, the dosage can depend on a number of factors including the requirements of the patient, the severity of the condition being treated, and the pharmacological activity of the compound being used. The determination of optimum dosages for a particular patient is well known to one of ordinary skill in the art.

If formulated as a fixed dose, such combination products employ the compounds of this invention within the dosage range described above and the other pharmaceutically active agent(s) within its approved dosage range. Compounds of the instant invention may alternatively be used sequentially with known pharmaceutically acceptable agent(s) when a combination formulation is inappropriate.

Representative pharmaceutical formulations containing a compound of Formula I or II are described below in the Pharmaceutical Composition Examples.

UTILITY

Certain compounds of Formula I have been tested using the assay described in Biological Example 1 and have been determined to be PI3K inhibitors. As such compounds of Formula I are useful for treating diseases, particularly cancer in which PI3K activity contributes to the pathology and/or symptomatology of the disease. For example, cancer in which PI3K activity contributes to its pathology and/or symptomatology include breast cancer, colon cancer, rectal cancer, endometrial cancer, gastric carcinoma, glioblastoma, hepatocellular carcinoma, small cell lung cancer, non-small cell lung cancer, melanoma, ovarian cancer, pancreatic cancer, prostate carcinoma, acute myelogenous leukemia (AML), chronic myelogenous leukemia (CML), and thyroid carcinoma, and the like.

Suitable in vitro assays for measuring PI3K activity and the inhibition thereof by compounds are known. Typically, the assay will measure PI3K-induced ATP consumption. For further details of an in vitro assay for measuring PI3K activity see Biological Examples, Example 1 infra. Cellular activity can be determined using assays as described in Biological Examples 2, 3, and 4 infra. Suitable in vivo models of cancer are known to those of ordinary skill in the art. For further details of in vivo assays see Biological Examples 5-10, infra. Examples describing the administration of a Compound of Formula I in combination with anticancer agents are described in Biological Examples 11-14, infra. Following the examples disclosed herein, as well as that disclosed in the art, a person of ordinary skill in the art can determine what combinations of a Compound of Formula I and anti-cancer agents would be effective for treating cancer.

Preparations of the Intermediates and Compounds of the Invention

Compounds of this invention can be made by the synthetic procedures described in WO 2007/044729, the disclosure of which is incorporated by reference herein.

The starting materials and reagents used in preparing these compounds are either available from commercial suppliers such as Aldrich Chemical Co. (Milwaukee, Wis.), or Bachem (Torrance, Calif.), or are prepared by methods known to those skilled in the art following procedures set forth in references such as Fieser and Fieser's Reagents for Organic Synthesis, Volumes 1-17 (John Wiley and Sons, 1991); Rodd's Chemistry of Carbon Compounds, Volumes 1-5 and Supplementals (Elsevier Science Publishers, 1989); Organic Reactions, Volumes 1-40 (John Wiley and Sons, 1991), March's Advanced Organic Chemistry, (John Wiley and Sons, 4^(th) Edition) and Larock's Comprehensive Organic Transformations (VCH Publishers Inc., 1989). These schemes are merely illustrative of some methods by which the compounds of this invention can be synthesized, and various modifications to these schemes can be made and will be suggested to one skilled in the art having referred to this disclosure. The starting materials and the intermediates of the reaction may be isolated and purified if desired using conventional techniques, including but not limited to filtration, distillation, crystallization, chromatography and the like. Such materials may be characterized using conventional means, including physical constants and spectral data.

Unless specified to the contrary, the reactions described herein take place at atmospheric pressure and over a temperature range from about −78° C. to about 150° C., in another embodiment from about 0° C. to about 125° C. and most specifically at about room (or ambient) temperature, e.g., about 20° C. Unless otherwise stated (as in the case of a hydrogenation), all reactions are performed under an atmosphere of nitrogen.

Prodrugs can be prepared by techniques known to one skilled in the art. These techniques generally modify appropriate functional groups in a given compound. These modified functional groups regenerate original functional groups by routine manipulation or in vivo. Amides and esters of the compounds of the present invention may be prepared according to conventional methods. A thorough discussion of prodrugs is provided in T. Higuchi and V. Stella, “Pro-drugs as Novel Delivery Systems,” Vol 14 of the A.C.S. Symposium Series, and in Bioreversible Carriers in Drug Design, ed. Edward B. Roche, American Pharmaceutical Association and Pergamon Press, 1987, both of which are incorporated herein by reference for all purposes.

The compounds of the invention, or their pharmaceutically acceptable salts, may have asymmetric carbon atoms or quaternized nitrogen atoms in their structure. Compounds of Formula I that may be prepared through the syntheses described herein may exist as single stereoisomers, racemates, and as mixtures of enantiomers and diastereomers. The compounds may also exist as geometric isomers. All such single stereoisomers, racemates and mixtures thereof, and geometric isomers are intended to be within the scope of this invention. Some of the compounds of the invention may exist as tautomers. For example, where a ketone or aldehyde is present, the molecule may exist in the enol form; where an amide is present, the molecule may exist as the imidic acid; and where an enamine is present, the molecule may exist as an imine. All such tautomers are within the scope of the invention.

In particular, in this application B can be 2-hydroxy-pyridinyl, also described as its structure:

Both 2-hydroxy-pyridinyl and the above structure 14 include, and are equivalent to, pyridin-2(1H)-one and its structure 15:

Regardless of which structure or which terminology is used, each tautomer is included within the scope of the Invention.

The present invention also includes N-oxide derivatives and protected derivatives of compounds of Formula I. For example, when compounds of Formula I contain an oxidizable nitrogen atom, the nitrogen atom can be converted to an N-oxide by methods well known in the art. When compounds of Formula I contain groups such as hydroxy, carboxy, thiol or any group containing a nitrogen atom(s), these groups can be protected with a suitable “protecting group” or “protective group”. A comprehensive list of suitable protective groups can be found in T. W. Greene, Protective Groups in Organic Synthesis, John Wiley & Sons, Inc. 1991, the disclosure of which is incorporated herein by reference in its entirety. The protected derivatives of compounds of Formula I can be prepared by methods well known in the art.

Methods for the preparation and/or separation and isolation of single stereoisomers from racemic mixtures or non-racemic mixtures of stereoisomers are well known in the art. For example, optically active (R)- and (S)-isomers may be prepared using chiral synthons or chiral reagents, or resolved using conventional techniques. Enantiomers (R- and S-isomers) may be resolved by methods known to one of ordinary skill in the art, for example by: formation of diastereoisomeric salts or complexes which may be separated, for example, by crystallization; via formation of diastereoisomeric derivatives which may be separated, for example, by crystallization, selective reaction of one enantiomer with an enantiomer-specific reagent, for example enzymatic oxidation or reduction, followed by separation of the modified and unmodified enantiomers; or gas-liquid or liquid chromatography in a chiral environment, for example on a chiral support, such as silica with a bound chiral ligand or in the presence of a chiral solvent. It will be appreciated that where a desired enantiomer is converted into another chemical entity by one of the separation procedures described above, a further step may be required to liberate the desired enantiomeric form. Alternatively, specific enantiomer may be synthesized by asymmetric synthesis using optically active reagents, substrates, catalysts or solvents or by converting on enantiomer to the other by asymmetric transformation. For a mixture of enantiomers, enriched in a particular enantiomer, the major component enantiomer may be further enriched (with concomitant loss in yield) by recrystallization.

In addition, the compounds of the present invention can exist in unsolvated as well as solvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like. In general, the solvated forms are considered equivalent to the unsolvated forms for the purposes of the present invention.

In Compounds of Formula I

the hydrogen on the —NHS(O)₂— group is highly acidic. Thus, intermediates leading to Compounds of Formula I, as well as Compounds of Formula I themselves, can be recovered as uncharged or zwitterionic molecules, or cationic salts such a sodium or potassium, depending on the substitutions on the B ring and on reaction conditions. In the examples that follow, unless otherwise specified, the final form of the compound was assumed to be the uncharged molecule in the absence of analytical techniques that would have determined otherwise.

Compounds of Formula I can be prepared using methods known to one of ordinary skill in the art. In another embodiment, fusion of appropriate reagents at 180° C. in the presence of a base such as K₂CO₃ and metallic copper is known to provide intermediates of formula 1 (see S. H. Dandegaonker and C. K. Mesta, J. Med. Chem. 1965, 8, 884).

Alternatively, the intermediate of formula 3 can be prepared according to the scheme below where each LG¹ is a leaving group (in one embodiment halo, in another embodiment chloro) and all other groups are as defined in the Detailed Description of the Invention.

In scheme 1, an intermediate of formula 3 can be prepared by briefly heating commercially available 2,3-dichloroquinoxaline and an intermediate of formula 2 (which are commercially available or can be prepared by one of ordinary skill in the art), a base such as K₂CO₃, in a solvent, such as DMF or DMSO. Upon completion (about 2 hours), the reaction mixture is then poured into water and followed by 2 N HCl. The product is then extracted into a solvent such as ethyl acetate and washed with water and brine. The organic layers are combined and dried over a drying agent such as sodium sulfate, filtered, and concentrated under vacuum.

The intermediate of formula 3 is then treated with an intermediate of formula 4 in a solvent such as DMF or p-xylene at reflux temperature. Upon completion of the reaction (about 16 hours or less), the reaction is allowed to cool, extracted into DCM, washed with 2 N HCl and brine, dried over a drying agent such as sodium sulfate or magnesium sulfate, filtered, and concentrated to give a compound of Formula I.

Alternatively, other methods to prepare quinoxaline derivatives are known to one skilled in the art and include, but are not limited to S. V. Litvinenko, V. I. Savich, D. D. Bobrovnik, Chem. Heterocycl. Compd. (Engl. Transl), 1994, 30, 340 and W. C. Lumma, R. D. Hartman, J. Med. Chem. 1981, 24, 93.

The following compounds were prepared in a manner similar to that described above.

Example 1

-   N-(3-{[2,5-bis(methoxy)phenyl]amino}quinoxalin-2-yl)-3-nitrobenzenesulfonamide.

Example 2

-   N-(3-{[2,5-bis(methoxy)phenyl]amino}quinoxalin-2-yl)-4-chlorobenzenesulfonamide.

Example 3

-   N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide.

Example 4

-   4-chloro-N-(3-chloroquinoxalin-2-yl)benzenesulfonamide.

Example 5

4-chloro-N-(3-(2,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. ¹H NMR (400 MHz, DMSO-d₆) δ 9.18 (s, 1H), 8.78 (s, 1H), 8.40-8.60 (m, 3H), 7.98 (t, 2H), 7.62 (d, 1H), 7.41 (m, 2H), 6.98 (d, 1H), 6.59 (d, 1H), 3.78 (s, 3H), 3.76 (s, 3H); MS (EI) m/z for C₂₂H₁₉N₅O₆S: 482.1 (MH⁺).

Example 6

N-(3-(2,5-dimethoxyphenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide. ¹H NMR (400 MHz, CDCl₃) δ 12.68 (br s, 1H), 9.18 (s, 1H), 8.55 (s, 1H), 8.08 (d, 2H), 7.98 (d, 1H), 7.78 (d, 2H), 7.62 (dd, 1H), 7.40 (m, 2H), 7.00 (d, 1H), 6.60 (dd, 1H), 3.78 (s, 6H); MS (EI) m/z for C₂₂H₁₉ClN₄O₄S: 471.1 (MH⁺).

Example 7

N-(3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)-4-methylphenyl)-2-(dimethylamino)acetamide. ¹H NMR (400 MHz, DMSO-d₆) δ 12.0 (br s, 1H), 10.6 (s, 1H), 10.0 (br s, 1H), 9.52 (s, 1H), 8.91 (d, 1H), 8.25 (d, 1H), 7.69 (dd, 1H), 7.47 (m, 1H), 7.39 (d, 1H), 7.16 (m, 3H), 6.01 (dd, 1H); MS (EI) m/z for C₂₆H₂₇ClN₆O₄S: 555 (MH⁺).

Compounds of Formula I where B is phenyl substituted with R^(3a) where R^(3a) is alkylamino or dialkylamino or B is heteroaryl substituted with R³ where R³ is amino, alkylamino, or dialkylamino, and all other groups are as defined in the Summary of the Invention can be prepared according to Scheme 2.

LG is a leaving group such as chloro. 5 is reacted with NHR^(a)R^(b) or HO—C₁-C₆-alkylene-NHR^(a)R^(b) where R^(a) and R^(b) are independently hydrogen or alkyl. The reaction is carried out in the presence of a base, such as KHCO₃, in a solvent such as DMF.

Compounds of Formula I where B is phenyl substituted with R^(1a) where R^(3a) is aminoalkyloxy, alkylaminoalkyloxy, or dialkylaminoalkyloxy or B is heteroaryl substituted with R³ where R³ is aminoalkyloxy, alkylaminoalkyloxy, or dialkylaminoalkyloxy, and all other groups are as defined in the Summary of the Invention can be prepared according to Scheme 3.

The reaction is carried out in the presence of a base such as NaH in a solvent such as DMF.

Compounds of Formula I where B is phenyl substituted with R^(3a) or B is heteroaryl substituted with R³ where R^(3a) and R³ are

-   -   i. —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)) where R⁷, R^(7a),         and R^(7b) are as defined in the Summary of the Invention;     -   ii. —NR⁹C(O)R^(9a) where R⁹ is as defined in the Summary of the         Invention;     -   iii. —NR¹¹C(O)NR^(11a)R^(11b) where R^(11a), R^(11a), and         R^(11b) are as defined in the Summary of the Invention;     -   iv. —NR¹³C(O)OR^(13a) where R¹³ and R^(13a) are as defined in         the Summary of the Invention;     -   v. —N(R¹⁸)C(O)—C₁-C₆-alkylene-N(R^(18b))C(O)R^(18a) where R¹⁸,         R^(18a), and R^(18b) are as defined in the Summary of the         Invention;     -   vi. —N(R²⁰)C(O)—C₁-C₆-alkylene-C(O)R^(20a) where R²⁰ and R^(20a)         as defined in the Summary of the Invention;     -   vii. —NR²¹S(O)₂—C₁-C₆-alkylene-N(R^(21b))R^(21a) where R²¹,         R^(21a), and R^(21b) are as defined in the Summary of the         Invention;     -   viii. —N(R²²)C(O)—C₀-C₆-alkylene-N(R^(22b))—N(R^(22c))(R^(22a)),         where R²², R^(22a) and R^(22b) are as defined in the Summary of         the Invention;     -   ix. —NR²⁴C(O)—C₁₋C₆-alkylene-OR^(24a) where R²⁴ and R^(24a) are         as defined in the Summary of the Invention;         and where the alkylene in R³ and R^(3a) are independently         optionally substituted as described in the Summary of the         Invention can be prepared according to Scheme 4 by reacting with         an intermediate of formula 9(a), 9(b), 9(c), 9(d), 9(e), 9(f),         or 9(g):     -   9(a) HOC(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)) where R^(a) is         R^(7a) or a N-protecting group, such as Boc or Fmoc;     -   9(b) HOC(O)R^(9a);     -   9(c) HOC(O)NR^(11a)R^(11b);     -   9(d) HOC(O)OR^(13a);     -   9(e) HOC(O)—C₁-C₆-alkylene-N(R^(18b))C(O)R^(18a);     -   9(f) HOC(O)—C₁-C₆-alkylene-C(O)R^(20a);     -   9(g) LG-S(O)₂—C₁₋C₆-alkylene-N(R^(21b))R^(a) where R^(a) is         R^(21a) or a N-protecting group, such as Boc or Fmoc.

-   R¹⁰⁰ in Scheme 4 is —C(O)R^(9a), —C(O)NR^(11a)R^(11b),     —C(O)OR^(13a), —C(O)—C₁-C₆-alkylene-N(R^(18b))C(O)R^(18a),     —C(O)—C₁-C₆-alkylene-C(O)R^(20a), or     —S(O)₂—C₁₋C₆-alkylene-N(R^(21b))R^(a). The reaction is carried out     under standard amide coupling conditions known to one of ordinary     skill in the art. In particular, the reaction is carried out in the     presence of a coupling agent such as HATU, a base such as DIEA, and     in a solvent such as DMF. Where applicable, the N-protecting group     is then removed using procedures known to one of ordinary skill in     the art, such as treating with acid where PG is Boc.

Proceeding as described for Scheme 4, compounds of the invention where B is phenyl substituted with R^(3a) or B is heteroaryl substituted with R³ where R^(3a) and R³ are

-   -   a) —C(O)NR⁸R^(8a);     -   b) —C(O)N(R¹⁰)—C₁-C₆-alkylene-N(R^(10a))R^(10b);     -   c) —C(O)R¹² where R¹² is an N-substituted heterocycloalkyl;     -   d) —C(O)N(R¹⁴)N(R^(14a))(R^(14b));     -   e) —C(O)N(R¹⁶)—C₁-C₆-alkylene-C(O)OR^(16a); or     -   f) —C(O)N(R¹⁹)—C₁-C₆-alkylene-C(O)R^(19a); or         can be prepared by exchanging the starting materials as         necessary. In particular, the intermediate of formula 11:

is used instead of 8.

Compounds of Formula I where B is phenyl substituted with R^(3a) or B is heteroaryl substituted with R³ where R^(3a) and R³ are —NHC(O)CH₂NR^(7a)R^(7b) where R^(7a) and R^(7b) are as defined in the Summary of the Invention can be prepared according to Scheme 5.

LG is a leaving group such as bromo or chloro. 12 is reacted with NH(R^(7b))R^(7a) in the presence of a base, such as DIEA, in a solvent such as ACN.

Compounds of Formula I can be prepared according to Scheme 6.

LG in Scheme 6 is a leaving group such as chloro. The reaction can be carried out by irradiating in a solvent such as DMA. Alternatively, the reaction can be carried out in the presence of acetic acid in a solvent such as DMA and by heating.

Example 8 6-chloro-N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)pyridine-3-sulfonamide

6-chloropyridine-3-sulfonamide. 6-chloropyridine-3-sulfonyl chloride (4.1 g, 19.3 mmol) was stirred in ammonium hydroxide (30 mL) at room temperature for 2 hr. The reaction mixture was diluted with EtOAc (150 mL) and any insoluble material filtered. The filtrate was transferred to a separatory funnel and the phases were separated. The aqueous phase was further extracted with EtOAc (1×15 mL). The combined EtOAc extractions were washed with H₂O (1×50 mL) and saturated NaCl (1×50 mL), dried over Na₂SO₄, and concentrated in vacuo to give 6-chloropyridine-3-sulfonamide (2.58 g, 69%). MS (EI) m/z for C₅H₅Cl₂N₂O₂S: 190.9 (MH⁻).

6-chloro-N-(3-chloroquinoxalin-2-yl)pyridine-3-sulfonamide. 2,3-dichloroquinoxaline (1.09 g, 5.48 mmol), 6-chloropyridine-3-sulfonamide (1.05 g, 5.45 mmol), K₂CO₃ (753 mg, 5.45 mmol) and dry DMSO (30 mL) were combined and heated to 150° C. with vigorous stirring for 3-4 hr. The reaction mixture was allowed to cool to room temperature, then poured into 1% AcOH in ice water (300 mL) with vigorous stirring. The resulting solids were filtered, washed with H₂O and dried under high vacuum to give 6-chloro-N-(3-chloroquinoxalin-2-yl)pyridine-3-sulfonamide (1.87 g, 96%). MS (EI) m/z for C₁₃H₈Cl₂N₄O₂S: 354.99 (MH⁺).

6-chloro-N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)pyridine-3-sulfonamide. 6-Chloro-N-(3-chloroquinoxalin-2-yl)pyridine-3-sulfonamide (775 mg, 2.2 mmol), 3,5-dimethoxyaniline (355 mg, 2.3 mmol) and toluene (12 mL) were combined and heated to 125° C. with stirring overnight. The reaction was allowed to cool to room temperature and diluted with Et₂O with vigorous stirring. The resulting solids were filtered, washed with Et₂O and dried to give 6-chloro-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)pyridine-3-sulfonamide (920 mg, 89%). ¹H NMR (400 MHz, DMSO-d₆) δ 12.20 (br s, 1H), 9.12 (d, 1H), 9.01 (br s, 1H), 8.53 (dd, 1H), 7.91 (br d, 1H), 7.77 (d, 1H), 7.60 (dd, 1H), 7.40 (m, 4H), 6.26 (m, 1H), 3.78 (s, 6H). MS (EI) m/z for C₂₁H₁₈ClN₅O₄S: 472.0 (MH⁺).

Example 9 N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-6-(2-(dimethylamino)-ethylamino)pyridine-3-sulfonamide

6-chloro-N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-pyridine-3-sulfonamide (100 mg, 0.21 mmol), prepared using procedures similar to those used in Example 8, KHCO₃ (40 mg, 0.40 mmol), N¹,N¹-dimethylethane-1,2-diamine (225 μL, 2.0 mmol) and dry DMF (1.0 mL) were combined and heated to 130° C. with stirring overnight. The reaction mixture was concentrated in vacuo and purified by preparative HPLC to give N-(3-(3,5-dimethoxy-phenylamino)-quinoxalin-2-yl)-6-(2-(dimethylamino)ethylamino)pyridine-3-sulfonamide (21.0 mg, 19%). ¹H NMR (400 MHz, DMSO-d₆) δ 8.76 (br s, 1H), 8.63 (d, 1H), 8.07 (dd, 1H), 7.40 (m, 1H), 7.34 (m, 1H), 7.28 (d, 2H), 7.14 (m, 4H), 6.47 (d, 1H), 6.12 (m, 1H), 3.75 (s, 6H), 3.35 (m, 2H), 3.14 (m, 2H), 2.74 (s, 6H). MS (EI) m/z for C₂₅H₂₉N₇O₄S: 524.1 (MH⁺).

Example 10

N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-6-(dimethylamino)pyridine-3-sulfonamide was prepared using procedures similar to those used in Example 9. ¹H NMR (400 MHz, DMSO-d₆) δ 12.00 (br s, 1H), 8.92 (br s, 1H), 8.74 (d, 1H), 8.10 (dd, 1H), 7.38 (br s, 1H), 7.54 (m, 1H), 7.33 (m, 4H), 6.70 (d, 1H), 6.22 (s, 1H), 3.77 (s, 6H), 3.08 (s, 6H). MS (EI) m/z for C₂₃H₂₄N₆O₄S: 481.1 (MH⁺).

Example 11 N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-6-(2-(dimethylamino)-ethoxy)pyridine-3-sulfonamide

N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)pyridine-3-sulfonamide (100 mg, 0.21 mmol), prepared using procedures similar to those described above in Example 1,2-(dimethylamino)ethanol (50 μL, 0.50 mmol) and dry DMF were combined and 60% NaH in oil (80 mg, 2.0 mmol) was added. The mixture was stirred at room temperature overnight. The reaction mixture was concentrated in vacuo and purified by preparative HPLC to give N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-6-(2-(dimethylamino)ethoxy)pyridine-3-sulfonamide (23 mg, 21%). ¹H NMR (400 MHz, DMSO-d₆) δ 8.78 (d, 1H), 8.73 (s, 1H), 8.38 (dd, 1H), 7.40 (dd, 1H), 7.31 (m, 3H), 7.14 (m, 2H), 6.85 (d, 1H), 6.12 (m, 1H), 4.56 (m, 2H), 3.76 (s, 6H), 3.43 (m, 2H), 2.77 (s, 6H). MS (EI) m/z for C₂₅H₂₈N₆O₅S: 525.1 (MH⁺).

Example 12 N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-6-oxo-1,6-dihydropyridine-3-sulfonamide

N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)pyridine-3-sulfonamide (220 mg, 0.47 mmol), prepared using procedures similar to those described above in Example 8, DMSO (5 mL), and 3N NaOH (5 mL) are combined and heated to 100° C. overnight with stirring. Upon cooling to room temperature, the reaction mixture was diluted with H₂O and the pH was adjusted to 7.0 with 1N HCl. The resulting solid was filtered, washed with H₂O, and air-dried. The solid was then sonicated in EtOAc, filtered, washed with EtOAc, and dried under high vacuum to give N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-6-oxo-1,6-dihydropyridine-3-sulfonamide (190 mg, 90%). ¹H NMR (400 MHz, DMSO-d₆) δ 12.23 (br s, 1H), 12.10 (br s, 1H), 8.97 (s, 1H), 8.23 (s, 1H), 7.95 (m, 2H), 7.59 (m, 1H), 7.37 (m, 4H), 6.43 (d, 1H), 6.25 (s, 1H), 3.77 (s, 6H). MS (EI) m/z for C₂₁H₁₉N₅O₅S: 454.0 (MH⁺).

Example 13

N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)-6-oxo-1,6-dihydropyridine-3-sulfonamide. The title compound was prepared according to the above Example 12. ¹H NMR (400 MHz, DMSO-d₆) δ 12.22 (br s, 1H), 12.10 (br s, 1H), 9.16 (s, 1H), 8.60 (s, 1H), 8.14 (d, 1H), 7.94 (m, 1H), 7.85 (dd, 1H), 7.62 (m, 1H), 7.40 (m, 3H) 6.69 (dd, 1H), 6.43 (d, 1H), 3.81 (s, 3H). MS (EI) m/z for C₂₀H₁₆ClN₅O₄S: 456.0 (MH⁻).

Example 14 3-amino-N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)benzenesulfonamide

N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide. A flask was charged with N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide (5 g, 13.7 mmol), prepared using procedures similar to those in Example 1, 3,5-dimethoxyaniline (4.2 g, 27.4 mmol), and 80 mL of xylene. The reaction mixture was stirred under an N₂ atmosphere at 150° C. for 3 hours, after which time, solvent was removed on a rotary evaporator, and 10 mL of Dichloromethane and 50 mL of methanol were added. The slurry was heated to reflux and filtered while hot, resulting in 4.6 g (69.7%) of N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide MS (EI) m/z for C₂₂H₁₉N₅O₆S: 482.2 (MH⁺).

Example 15 3-amino-N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)benzenesulfonamide

A flask was charged with N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-3-nitro-benzenesulfonamide (3.4 g, 7.06 mmol), prepared using procedures similar to those in Example 14, tin chloride solvate (6.4 g, 28.2 mmol), and 30 mL of DMA. A few drops of water were added and the reaction mixture was stirred at 80° C. for 3 hours, after which time, solvent was removed on a rotary evaporator, and 50 mL of water and 10 mL of Methanol were added. The slurry was filtered, and the filtrate was washed with MeOH, water, and diethyl ether (20 mL of each), resulting in 3.25 g 3-amino-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. ¹H NMR (400 MHz, DMSO) δ 12.2 (br s, 1H), 8.85 (s, 1H), 7.90 (br s, 1H), 7.50-7.60 (m, 1H), 7.3-7.4 (m, 4H), 7.2 (m, 3H), 6.74 (m, 1H), 6.24 (m, 1H), 5.56 (br s, 2H), 3.76 (s, 6H). MS (EI) m/z for C₂₂H₂₁N₅O₄S: 452.0 (MH⁺).

The following compounds were made using procedures similar to those used in Example 15.

Example 16

Proceeding as above, 3-amino-N-(3-(2,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide was prepared. ¹H NMR (400 MHz, DMSO) δ 12.4 (br s, 1H), 9.20 (s, 1H), 8.56 (d, 1H), 7.95 (d, 1H), 7.62 (m, 1H), 7.38 (m, 2H), 7.24 (q, 2H), 7.14 (d, 1H), 6.98 (d, 1H), 6.8 (m, 1H), 6.60 (m, 1H), 5.6 (br s, 2H), 3.78 (d, 6H). MS (EI) m/z for C₂₂H₂₁N₅O₄S: 452.3 (MH⁺).

Example 17

Proceeding as above, 3-amino-N-(3-(2-chloro-5-hydroxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide was prepared. MS (EI) m/z for C₂₀H₁₆ClN₅O₃S 1.0×C₂H₁O₂F₃: 442.2, 444.2 (MH⁺).

Example 18

Proceeding as above, 3-amino-N-(3-(6-methoxyquinolin-8-ylamino)quinoxalin-2-yl)benzenesulfonamide was prepared. MS (EI) m/z for C₂₄H₂₀N₆O₃S: 473.0 (MH⁺).

Example 19

3-amino-N-(3-(3-fluoro-5-methoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₁H₁₈FN₅O₃S: 439.99 (MH⁺).

Example 20

3-amino-N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₁H₁₈ClN₅O₃S: 457.02 (MH⁺).

Example 21

3-amino-N-(3-(5-methoxy-2-methyl-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₂H₂₁N₅O₃S: 436.32 (MH⁺).

Example 22a and Example 22b

3-amino-N-(3-(3-methoxy-5-nitro-phenylamino)quinoxalin-2-yl)benzenesulfonamide and 3-amino-N-(3-(3-amino-5-methoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide

To a mixture of N-(3-{[3-(methyloxy)-5-nitrophenyl]amino}quinoxalin-2-yl)-3-nitrobenzenesulfonamide (400 mg), THF (2 mL) and EtOH (2 mL) was added formic acid (938 μL), potassium formate (203 mg). After the mixture was flushed with N₂, 10% wt Pd/C (50 mg) was added. The resulting mixture was heated at 60° C. with stirring. LC/MS analysis indicated that the reaction mixture contained the complete reduced di-amino compound as the major product and the partially reduced mono-amino compound as a minor product. A portion of the crude mixture was purified by HPLC to give the two products. Product A: 3-amino-N-(3-(3-methoxy-5-nitro-phenylamino)quinoxalin-2-yl)benzenesulfonamide. ¹H NMR (400 MHz, DMSO) δ 12.2 (br s, 1H), 9.51 (s, 1H), 8.77 (s, 1H), 8.21 (s, 1H), 7.92 (s, 1H), 7.48 (m, 1H), 7.43-7.38 (m, 3H), 7.24-7.16 (m, 3H), 6.75 (d, 1H), 5.57 (br s, 2H), 3.90 (s, 3H). MS (EI) for C₂₁H₁₈N₆O₅S: 467.00 (MH+). Product B: 3-amino-N-(3-(3-amino-5-methoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. ¹H NMR (400 MHz, DMSO) δ 12.0 (br. s, 1H), 8.53 (s, 1H), 7.84 (s, 1H), 7.56 (d, 1H), 7.37-7.30 (m, 2H), 7.21-7.17 (m, 3H), 6.87 (s, 1H), 6.81 (s, 1H), 6.74 (br s, 2H), 5.91 (s, 1H), 5.56 (br s, 3H), 3.69 (s, 3H). MS (EI) for C₂₁H₂₀N₆O₃S: 437.2 (MH⁺).

Example 23a and Example 23b N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-3-(hydroxyamino)-benzenesulfonamide and 3-amino-N-(3-{[3,5-(dimethoxy)phenyl]amino}quinoxalin-2-yl)benzenesulfonamide

To a solution N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide (1.3 g) in 20 mL of THF and 10 mL of MeOH was added 10% wt Pd/C (100 mg). The mixture was stirred under a H₂ balloon overnight. A portion of the reaction mixture was taken out and filtered, then purified by HPLC to afford two products. Product A: N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-(hydroxyamino)benzenesulfonamide. MS (EI) for C₂₂H₂₁N₅O₅S: 468.1 (MH⁺). Product B: 3-amino-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. ¹H NMR (400 MHz, DMSO) δ 12.2 (br s, 1H), 8.85 (s, 1H), 7.90 (br s, 1H), 7.50-7.60 (m, 1H), 7.3-7.4 (m, 4H), 7.2 (m, 3H), 6.74 (m, 1H), 6.24 (m, 1H), 5.56 (br s, 2H), 3.76 (s, 6H). MS (EI) for C₂₂H₂₁N₅O₄S: 452.0 (MH⁺).

Example 24 (S)-2-amino-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)propanamide hydrochloride

(S)-tert-butyl 1-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenylamino)-1-oxopropan-2-ylcarbamate. 3-amino-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide (1.1 mmol, 500 mg), prepared using procedures similar to those described above in Example 15, (L)-Boc-Ala-OH (1.5 mmol, 284 mg), dichloromethane (15 mL), DMF (10 mL), DIEA (2 mmol, 330 μL), and HATU (2 mmol, 760 mg) stirred at room temperature over night. The crude mixture was column purified using 1/1 ethyl acetate/hexanes on silica to gave 160 mg.

(S)-2-amino-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)propanamide hydrochloride. 4 N HCl is dioxane (10 mL) was added to a solution of (S)-tert-butyl 1-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenylamino)-1-oxopropan-2-ylcarbamate (160 mg) and DCM (15 mL). The mixture was stirred at room temperature for 3 hours. The solvent decanted and ether added to the solid, ether decanted to gave 80 mg product as HCl salt. ¹H NMR (400 MHz, CD₃OD) δ 8.50-8.49 (t, 1H), 7.89-7.87 (m, 1H), 7.74-7.72 (m, 1H), 7.61-7.5 (m, 3H), 7.40-7.36 (m, 2H), 7.21-7.20 (d, 2H), 6.23-6.21 (t, 1H), 4.09-4.03 (q, 1H), 3.78 (s, 6H), 1.60-1.58 (d, 3H); MS (EI) m/z for C₂₅H₂₆N₆O₅S.HCl: 523.1 (MH⁺).

The following compounds were prepared as the free amine and/or HCl salt using procedures similar to those in Example 24. Where the deprotection step is not necessary, Step B in the above scheme was not preformed.

Example 25

N-(2-chloro-5-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(methylamino)acetamide. The title compound was prepared according to the Examples above. ¹H NMR (400 MHz, DMSO-d₆) δ 10.50 (s, 1H), 9.14 (s, 1H), 9.03 (m, 2H), 8.63 (d, 1H), 8.44 (d, 1H), 7.98 (m, 1H), 7.91 (dd, 1H), 7.80 (d, 1H), 7.67 (m, 1H), 7.44 (m, 3H), 6.71 (dd, 1H), 4.06 (m, 2H), 3.83 (s, 3H), 2.64 (t, 3H). MS (EI) m/z for C₂₄H₂₂Cl₂N₆O₄S: 561.0 (MH⁺).

Example 26

(S)-2-amino-N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)propanamide hydrochloride. ¹H NMR (400 MHz, CD₃OD) δ 8.72-8.71 (d, 1H), 8.48-8.46 (t, 1H), 7.86-7.84 (m, 1H), 7.80-7.78 (m, 1H), 7.63-7.59 (m, 2H), 7.58-7.55 (t, 1H), 7.41-7.38 (m, 2H), 7.24-7.22 (d, 1H), 6.60-6.58 (dd, 1H), 4.10-4.04 (q, 1H), 3.83 (s, 3H), 1.61-1.60 (d, 3H); MS (EI) m/z for C₂₄H₂₃ClN₆O₄S.HCl: 527.2 (MH⁺).

Example 27

(S)-2-amino-N-(3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)butanamide hydrochloride. ¹H NMR (400 MHz, CD₃OD) δ 8.74-8.73 (d, 1H), 8.80-8.47 (t, 1H), 7.87-7.85 (m, 1H), 7.80-7.78 (m, 1H), 7.67-7.61 (m, 2H), 7.59-7.55 (t, 1H), 7.42-7.39 (m, 2H), 7.26-7.24 (d, 1H), 6.62-6.59 (dd, 1H), 3.96-3.93 (t, 1H), 3.84 (s, 3H), 2.02-1.94 (m, 2H, 1.09-1.06 (t, 3H); MS (EI) m/z for C₂₅H₂₅ClN₆O₄S.HCl: 541.3 (MH⁺).

Example 28

(S)—N-(3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)pyrrolidine-2-carboxamide hydrochloride. ¹H NMR (400 MHz, CD₃OD) δ 8.78-8.77 (d, 1H), 8.47-8.46 (t, 1H), 7.87-7.85 (m, 1H), 7.80-7.75 (m, 1H), 7.69-7.65 (m, 2H), 7.59-7.55 (t, 1H), 7.45-7.41 (m, 2H), 7.31-7.28 (d, 1H), 6.65-6.63 (dd, 1H), 4.42-4.38 (m, 1H), 3.86 (s, 3H), 3.48-3.42 (m, 2H), 2.55-2.49 (m, 1H), 2.18-2.08 (m, 3H); MS (EI) m/z for C₂₆H₂₅ClN₆O₄S.HCl: 553.3 (MH⁺).

Example 29

(S)—N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)pyrrolidine-2-carboxamide hydrochloride. ¹H NMR (400 MHz, CD₃OD) δ 10.62 (br s, 1H), 8.50-8.49 (t, 1H), 7.90-7.87 (m, 1H), 7.76-7.73 (m, 1H), 7.63-7.58 (m, 3H), 7.43-7.35 (m, 2H), 7.14 (s, 2H), 6.27-6.26 (t, 1H), 4.43-4.38 (m, 1H), 3.78 (s, 6H), 3.48-3.41 (m, 1H), 3.40-3.36 (m, 1H(, 2.54-2.48 (m, 1H), 2.19-2.05 (m, 3H); MS (EI) m/z for C₂₇H₂₈N₆O₅S.HCl: 549.3 (MH⁺).

Example 30

(R)-2-amino-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-hydroxypropanamide hydrochloride. ¹H NMR (400 MHz, CD₃OD) δ 8.49-8.48 (t, 1H), 7.89-7.87 (m, 1H), 7.75-7.72 (m, 1H), 7.65-7.62 (m, 2H), 7.62-7.55 (t, 1H), 7.44-7.38 (m, 2H), 7.23-7.22 (d, 2H), 6.27-6.26 (t, 1H), 4.07-4.05 (m, 1H), 3.99-3.93 (m, 2H), 3.80 (s, 6H); MS (EI) m/z for C₂₅H₂₆N₆O₆S.HCl: 539.1 (MH⁺).

Example 31

N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)piperidine-3-carboxamide hydrochloride. ¹H NMR (400 MHz, CD₃OD) δ 8.79-8.78 (d, 1H), 8.45 (m, 1H), 7.83-7.81 (d, 1H), 7.76-7.74 (m, 1H), 7.636 (m, 2H), 7.54-7.50 (t, 1H), 7.41 (m, 2H), 7.30-7.28 (d, 1H), 6.65-6.62 (dd, 1H), 3.86 (s, 3H), 3.40-3.32 (m, 2H), 3.20-3.13 (m, 3H), 2.93 (m, 1H), 2.15-2.11 (m, 1H), 1.98-1.93 (m, 2H), 1.83 (m, 1H); MS (EI) m/z for C₂₇H₂₇ClN₆O₄S.HCl: 567.3 (MH⁺).

Example 32

(S)-2-amino-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)butanamide hydrochloride. MS (EI) m/z for C₂₆H₂₈N₆O₅S.HCl: 537.1 (MH⁺).

Example 33

(R)—N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)pyrrolidine-2-carboxamide hydrochloride. MS (EI) m/z for C₂₇H₂₈N₆O₅S.HCl: 549.1 (MH⁺).

Example 34

(R)—N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)pyrrolidine-2-carboxamide hydrochloride. MS (EI) m/z for C₂₆H₂₅ClN₆O₄S.HCl: 553 (MH⁺).

Example 35

(R)-2-amino-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)propanamide. ¹H NMR (400 MHz, DMSO-d₆) δ 10.2 (br s, 1H), 8.82 (s, 1H), 8.27 (m, 1H), 7.75 (m, 2H), 7.33 (m, 5H), 7.13 (m, 2H), 6.14 (t, 1H), 3.77 (s, 6H), 1.39 (d, 3H); MS (EI) m/z for C₂₅H₂₆N₆O₅S: 523 (MH⁺).

Example 36

N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(methylamino)acetamide. ¹H NMR (400 MHz, DMSO-d₆) δ 10.6 (s, 1H), 9.48 (s, 1H), 8.95 (br s, 1H), 8.75 (br s, 1H), 8.19 (br s, 1H), 7.77 (dd, 1 H), 7.69 (dd, 1H), 7.41 (m, 4H), 7.17 (m, 2H), 6.60 (dd, 1H), 3.91 (s, 2H), 3.82 (s, 6 H), 2.62 (s, 3H); MS (EI) m/z for C₂₄H₂₃ClN₆O₄S: 527 (MH⁺).

Example 37

(R)-2-amino-N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)propanamide. ¹H NMR (400 MHz, DMSO-d₆) δ 10.5 (s, 1H), 9.47 (s, 1H), 8.95 (d, 1H), 8.22 (d, 2H), 8.14 (br s, 2H), 7.76 (m, 2H), 7.40 (m, 4H), 7.17 (m, 2H), 6.60 (m, 1H), 3.97 (q, 1H), 3.96 (s, 3H), 1.45 (d, 3H); MS (EI) m/z for C₂₄H₂₃ClN₆O₄S: 527 (MH⁺).

Example 38

2-amino-N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-methylpropanamide. ¹H NMR (400 MHz, DMSO-d₆) δ 10.1 (s, 1H), 9.46 (s, 1H), 8.95 (d, 1H), 8.50 (br s, 1H), 8.27 (m, 1H), 7.81 (m, 2H), 7.47 (m, 1H), 7.37 (m, 3H), 7.17 (m, 2H), 6.61 (dd, 1H), 3.83 (s, 3H), 1.60 (s, 6H); MS (EI) m/z for C₂₅H₂₅ClN₆O₄S: 541 (MH⁺).

Example 39

2-amino-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-methylpropanamide. ¹H NMR (400 MHz, DMSO-d₆) δ 10.33 (s, 1H), 8.89 (s, 1H), 8.32 (br s, 4H), 7.92 (m, 3H), 7.59 (m, 2H), 7.37 (m, 4H), 6.24 (s, 1H), 3.76 (s, 6H), 1.61 (s, 6H); MS (EI) m/z for C₂₆H₂₈N₆O₅S: 537 (MH⁺).

Example 40

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-4-methylphenyl)-2-(dimethylamino)acetamide. ¹H NMR (400 MHz, DMSO-d₆) δ 10.58 (s, 1H), 9.80 (br s, 1H), 8.85 (s, 1H), 8.25 (s, 1H), 7.67 (dd, 1H), 7.30 (m, 7H), 6.16 (m, 1H), 4.02 (br s, 2H), 3.77 (s, 6H), 2.81 (s, 6H), 2.54 (s, 3H); MS (EI) m/z for C₂₇H₃₀N₆O₅S: 551 (MH⁺).

Example 41 N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-((2-(dimethylamino)ethyl)(methyl)amino)acetamide. ¹H NMR (400 MHz, DMSO-d₆) δ 10.0 (s, 1H), 9.48 (s, 1H), 8.96 (d, 1H), 8.16 (m, 1H), 7.76 (m, 2H), 7.39 (m, 4H), 7.17 (m, 2H), 6.61 (dd, 1H), 3.82 (s, 3H), 3.40 (br s, 2H), 2.94 (br s, 2H), 2.71 (br t, 2H), 2.60 (s, 6H), 2.33 (s, 3H); MS (EI) m/z for C₂₈H₃₂ ^(ClN) ₇O₄S: 598 (MH⁺). Example 42

2-amino-N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. ¹H NMR (400 MHz, DMSO-d₆) δ 10.5 (s, 1H), 9.48 (s, 1H), 8.94 (s, 1H), 8.15 (s, 1H), 8.06 (br s, 3H), 7.74 (m, 2H), 7.39 (m, 4H), 7.18 (m, 2H), 6.61 (dd, 1H), 3.83 (s, 3H), 3.77 (s, 2H); MS (EI) m/z for C₂₃H₂₁ClN₆O₄S: 513 (MH⁺).

Example 43

N-(3-(N-(3-(2-acetyl-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(dimethylamino)acetamide. NMR (400 MHz, DMSO-d₆) δ 12.4 (s, 1H), 10.5 (s, 1H), 9.27 (s, 1H), 8.25 (s, 1H), 8.01 (d, 1H), 7.82 (d, 1H), 7.71 (d, 1H), 7.42 (m, 3H), 7.21 (m, 2H), 6.63 (dd, 1H), 3.91 (m, 5H), 2.75 (s, 6H), 2.61 (s, 3H); MS (EI) m/z for C₂₇H₂₈N₆O₅S: 549 (MH⁺).

Example 44

N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)formamide. NMR (400 MHz, DMSO-d₆) δ 12.6 (s, 1H), 10.5 (s, 1H), 9.16 (s, 1H), 8.53 (br s, 1H), 8.35 (m, 2H), 8.02 (s, 1H), 7.56 (m, 7H), 6.70 (dd, 1H), 3.83 (s, 3H); MS (EI) m/z for C₂₂H₁₈ClN₅O₄S: 484 (MH⁺).

Example 45

2-amino-N-(5-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-2-methylphenyl)acetamide. ¹H NMR (400 MHz, DMSO-d₆) δ 12.4 (s, 1 H), 10.1 (br s, 1H), 8.82 (s, 1H), 8.20 (m, 3H), 7.82 (m, 1H), 7.30 (m, 6H), 6.20 (s, 1 H), 3.85 (s, 2H), 3.77 (s, 6H), 2.26 (s, 3H); MS (EI) m/z for C₂₅H₂₆N₆O₅S: 523 (MH⁺).

Example 46

N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-methyl-2-(methylamino)propanamide. NMR (400 MHz, DMSO-d₆) δ 10.09 (s, 1H), 9.46 (s, 1H), 8.95 (m, 3H), 8.28 (s, 1H), 7.81 (m, 2H), 7.41 (m, 4H), 7.17 (m, 2H), 6.60 (dd, 1H), 3.82 (s, 3H), 2.53 (s, 3H), 1.60 (s, 6H); MS (EI) m/z for C₂₆H₂₇ClN₆O₄S: 555 (MH⁺).

Example 47

(S)—N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(methylamino)propanamide. ¹H NMR (400 MHz, DMSO-d₆) δ 10.61 (s, 1H), 9.47 (s, 1H), 8.95 (s, 1H), 8.82 (br s, 2H), 8.27 (m, 1H), 7.74 (m, 2 H), 7.42 (m, 4H), 7.17 (m, 2H), 6.60 (dd, 1H), 3.90 (m, 1H), 3.82 (s, 3H), 2.59 (s, 3 H), 1.49 (d, 3H); MS (EI) m/z for C₂₅H₂₅ClN₆O₄S: 541 (MH⁺).

Example 48

3-amino-N-(5-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)-2-methylphenyl)propanamide. ¹H NMR (400 MHz, DMSO-d₆) δ 12.25 (s, 1H), 9.77 (s, 1H), 8.82 (s, 1H), 7.84 (m, 5H), 7.50 (d, 1H), 7.37 (m, 5H), 6.22 (m, 1H), 3.74 (s, 6H), 3.08 (m, 2H), 2.77 (m, 2H), 2.27 (s, 3H); MS (EI) m/z for C₂₆H₂₈N₆O₅S: 537 (MH⁺).

Example 49

1-amino-N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)cyclopropanecarboxamide. ¹H NMR (400 MHz, DMSO-d₆) δ 9.54 (br s, 1H), 9.42 (s, 1H), 8.91 (s, 1H), 8.21 (s, 1H), 8.20 (br s, 2H), 7.81 (m, 2 H), 7.48 (m, 4H), 7.22 (m, 2H), 6.61 (dd, 1H), 3.82 (s, 3H), 1.63 (m, 2H), 1.26 (m, 2 H); MS (EI) m/z for C₂₅H₂₃ClN₆O₄S: 539 (MH⁺).

Example 50

(S)-2-amino-N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-6-(dimethylamino)hexanamide. ¹H NMR (400 MHz, DMSO-d₆) δ 9.47 (br s, 1H), 8.95 (d, 1H), 8.26 (m, 1H), 7.73 (m, 2H), 7.30 (m, 4H), 7.26 (m, 4H), 7.16 (m, 2H), 6.59 (dd, 1H), 3.82 (s, 3H), 3.34 (m, 1H), 2.20 (m, 2H), 2.09 (s, 6 H), 1.50 (m, 6H); MS (EI) m/z for C₂₉H₃₄ClN₇O₄S: 610 (MH⁺).

Example 51

1-amino-N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)cyclopentanecarboxamide. ¹H NMR (400 MHz, DMSO-d₅) δ 10.12 (br s, 1H), 9.46 (s, 1H), 8.95 (d, 1H), 8.26 (m, 1H), 8.16 (m, 3H), 7.84 (m, 2 H), 7.35 (m, 6H), 6.60 (dd, 1H), 3.82 (s, 3H), 2.34 (m, 2H), 1.91 (m, 6H); MS (EI) m/z for C₂₇H₂₇ClN₆O₄S: 567 (MH⁺).

Example 52

N-(5-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)-2-methylphenyl)-2-(dimethylamino)acetamide. ¹H NMR (400 MHz, DMSO-d₆) δ 12.0 (br s, 1H), 9.98 (s, 1H), 9.43 (s, 1H), 8.91 (m, 1H), 8.08 (s, 1H), 7.84 (dd, 1H), 7.32 (m, 6H), 6.61 (dd, 1H), 4.07 (s, 2H), 3.82 (s, 3H), 2.82 (s, 6H), 2.21 (s, 3H); MS (EI) m/z for C₂₆H₂₇ClN₆O₄S: 555 (MH⁺).

Example 53

1-amino-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)cyclobutanecarboxamide. ¹H NMR (400 MHz, DMSO-d₆) δ 10.34 (br s, 1H), 8.81 (s, 1H), 8.49 (br s, 3H), 8.34 (s, 1H), 7.83 (m, 2H), 7.43 (m, 3H), 7.31 (m, 2H), 7.16 (m, 2H), 6.16 (s, 1H), 3.77 (s, 6H), 2.83 (m, 2H), 2.25 (m, 3 H), 2.05 (m, 1H); MS (EI) m/z for C₂₇H₂₈N₆O₅S: 549 (MH⁺).

Example 54

N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-3-(3-(2-(dimethylamino)ethyl)ureido)benzenesulfonamide. ¹H NMR (400 MHz, DMSO-d₆) δ 8.91 (br s, 1H), 8.81 (s, 1H), 8.08 (s, 1H), 7.60 (s, 1H), 7.38 (m, 9H), 6.28 (m, 1H), 6.15 (s, 1H), 3.78 (s, 6H), 3.40 (m, 2H), 3.08 (m, 2H), 2.74 (s, 6H); MS (EI) m/z for C₂₇H₃₁N₇O₅S: 566 (MH⁺).

Example 55

1-amino-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)cyclopentanecarboxamide. ¹H NMR (400 MHz, DMSO-d₆) δ 12.40 (br s, 1H), 10.58 (s, 1H), 8.46 (m, 4H), 7.80 (m, 3H), 7.59 (m, 2H), 7.34 (m, 4 H), 6.25 (m, 1H), 3.76 (s, 6H), 2.35 (m, 2H), 1.90 (m, 8H); MS (EI) m/z for C₂₈H₃₀N₆O₅S: 563 (MH⁺).

Example 56

1-amino-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)cyclopropanecarboxamide. ¹H NMR (400 MHz, DMSO-d₆) δ 9.54 (br s, 1H), 8.84 (s, 1H), 8.29 (s, 1H), 7.75 (m, 2H), 7.39 (m, 6H), 7.17 (m, 2H), 6.16 (m, 1H), 3.78 (s, 6H), 1.52 (m, 2H), 1.17 (m, 2H); MS (EI) m/z for C₂₆H₂₆N₆O₅S: 535 (MH⁺).

Example 57 2-(dimethylamino)ethyl 3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenylcarbamate. ¹H NMR (400 MHz, DMSO-d₆) δ 9.78 (br s, 1H), 8.79 (s, 1H), 8.19 (s, 1H), 7.66 (d, 1H), 7.31 (m, 9H), 6.14 (m, 1H), 4.17 (t, 2H), 3.78 (s, 6H), 2.54 (t, 2H), 2.21 (s, 6H): MS (EI) m/z for C₂₇H₃₀N₆O₆S: 567 (MH⁺). Example 58

4-amino-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)tetrahydro-2H-pyran-4-carboxamide. ¹H NMR (400 MHz, DMSO-d₆) δ 12.2 (br s, 1H), 10.6 (s, 1H), 8.74 (m, 5H), 7.93 (m, 2H), 7.47 (m, 6H), 6.24 (m, 1H), 3.77 (m, 10H), 2.45 (m, 2H), 1.81 (m, 2H); MS (EI) m/z for C₂₈H₃₀N₆O₆S: 579 (MH⁺).

Example 59

N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)-N-3-(2-(dimethylamino)ethyl)benzene-1,3-disulfonamide. ¹H NMR (400 MHz, DMSO-d₆) δ 9.35 (m, 2H), 8.92 (m, 1H), 8.64 (s, 1H), 8.30 (m, 1H), 8.11 (s, 1H), 7.86 (m, 1H), 7.68 (m, 1H), 7.49 (s, 1H), 7.42 (m, 2H), 7.21 (m, 2H), 6.61 (m, 1H), 3.82 (s, 3H), 3.05 (m, 4H), 2.74 (s, 6H); MS (EI) m/z for C₂₅H₂₇ClN₆O₅S₂: 591 (MH⁺).

Example 60

N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)-N3-(3-(dimethylamino)propyl)benzene-1,3-disulfonamide. ¹H NMR (400 MHz, DMSO-d₆) δ 9.38 (m, 2H), 8.90 (m, 1H), 8.60 (s, 1H), 8.32 (m, 1H), 8.12 (s, 1H), 7.88 (m, 1H), 7.72 (m, 1H), 7.59 (s, 1H), 7.40 (m, 2H), 7.20 (m, 2H), 6.67 (m, 1H), 3.82 (s, 3H), 2.97 (m, 2H), 2.78 (m, 2H), 2.71 (s, 6H), 1.70 (m, 2H); MS (EI) m/z for C₂₆H₂₉ClN₆O₅S₂: 605 (MH⁺).

Example 61

N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-4-methylphenyl)-2-(methylamino)acetamide. MS (EI) m/z for C₂₅H₂₅ClN₆O₄S: 541.0 (MH⁺).

Example 62

(S)-2-amino-N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-4-methylphenyl)propanamide. MS (EI) m/z for C₂₅H₂₅ClN₆O₄S: 541.2 (MH⁺).

Example 63

(R)-2-amino-N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-4-methylphenyl)propanamide. MS (EI) m/z for C₂₅H₂₅ClN₆O₄S: 541.0 (MH⁺).

Example 64

(S)—N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(methylamino)propanamide. MS (EI) m/z for C₂₆H₂₈N₆O₅S: 537.1 (MH⁺).

Example 65

(R)—N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(methylamino)propanamide. MS (EI) m/z for C₂₅H₂₅ClN₆O₄S: 541.1 (MH⁺).

Example 66

(R)—N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(methylamino)propanamide. MS (EI) m/z for C₂₆H₂₈N₆O₅S: 537.3 (MH⁺).

Example 67

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)piperidine-2-carboxamide. MS (EI) m/z for C₂₈H₃₀N₆O₅S: 563.1 (MH⁺).

Example 68

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-(dimethylamino)ethylamino)acetamide. MS (EI) m/z for C₂₈H₃₃N₇O₅S: 580.1 (MH⁺).

Example 69

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(4-(methylamino)piperidin-1-yl)acetamide. MS (EI) m/z for C₃₀H₃₅N₇O₆S: 606.1 (MH⁺).

Example 70

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(4-(dimethylamino)piperidin-1-yl)acetamide. MS (EI) m/z for C₃₁H₃₇N₇O₅S: 620.1 (MH⁺).

Example 71

N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(dimethylamino)acetamide. ¹H NMR (400 MHz, DMSO) δ 12.4 (br s, 1H), 10.9 (s, 1H), 9.8 (s, 1H), 8.9 (s, 1H), 8.3 (br s, 1H), 7.9 (d, 2H), 7.8 (d, 1H), 7.6 (t, 2H), 7.4 (q, 2H), 7.3 (s, 1H), 6.25 (s, 1H), 4.15 (s, 2H), 3.8 (s, 6H), 2.9 (s, 6H). MS (EI) m/z for C₂₆H₂₈N₆O₅S 2.0×C₂H₁O₂F₃: 537.1 (MH⁺).

Example 72

N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(ethylamino)acetamide. ¹H NMR (400 MHz, DMSO) δ 10.8 (s, 1H), 9.20 (s, 1H), 8.84 (br s, 2H), 8.64 (br s, 1H), 8.30 (s, 1H), 7.9-8.0 (br s, 1H), 7.80 (t, 2H), 7.55-7.68 (m, 2H), 7.4 (d, 3H), 6.70 (m, 1H), 3.97 (br s, 2H), 3.83 (s, 3H), 3.04 (br s, 2H), 1.3 (t, 3H). MS (EI) m/z for C₂₅H₂₅ClN₆O₄S 2.0×C₂H₁O₂F₃: 541.3, 543.2 (MH⁺).

Example 73 2-(azetidin-1-yl)-N-(3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. ¹H NMR (400 MHz, DMSO) δ 10.8 (s, 1H), 10.2 (s, 1H), 9.2 (s, 1H), 8.7 (s, 1H), 8.3 (s, 1H), 7.9-8.0 (br s, 1H), 7.80 (d, 1H), 7.72 (d, 1H), 7.65 (br s, 1H), 7.56 (t, 1H), 7.40 (d, 3H), 6.70 (m, 1H), 4.28 (s, 2H), 4.15 (m, 4H), 3.82 (s, 3H), 2.32 (br s, 1H). MS (EI) m/z for C₂₆H₂₅ClN₆O₄S 2.0×C₂H₁O₂F₃: 553.3, 555.2 (MH⁺). Example 74

N-(3-(N-(3-(2-bromo-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(methylamino)acetamide. The title compound was prepared according to the Examples above. ¹H NMR (400 MHz, DMSO) δ 10.6 (s, 1H), 9.5 (s, 1H), 8.95 (d, 1H), 8.18 (t, 1H), 7.78 (m, 1H), 7.70 (m, 1H), 7.54 (d, 1H), 7.46 (m, 1H), 7.38 (t, 1H), 7.32 (d, 1H), 7.12-7.22 (m, 2H), 6.56 (m, 1H), 3.90 (s, 2H), 3.82 (s, 3H), 2.62 (s, 3H). MS (EI) m/z for C₂₄H₂₃BrN₆O₄S: 572.77, 570.90 (MH⁺).

Example 75

2-(dimethylamino)-N-(3-(N-(3-(6-methoxy-quinolin-8-ylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. The title compound was prepared according to the Examples above. ¹H NMR (400 MHz, DMSO) δ 10.9 (s, 1H), 10.6 (s, 1H), 9.13 (s, 1H), 8.80 (d, 1H), 8.26-8.30 (m, 2H), 7.85 (d, 1H), 7.70 (d, 1H), 7.60 (q, 1H), 7.54 (m, 1H), 7.44 (t, 2H), 7.20 (t, 2H), 6.80 (d, 1H), 4.00 (s, 2H), 3.94 (s, 3H), 2.78 (s, 6H). MS (EI) m/z for C₂₈H₂₇N₇O₄S: 558.3 (MH⁺).

Example 76

N-(3-(N-(3-(2-bromo-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(dimethylamino)acetamide. NMR (400 MHz, DMSO) δ 10.6 (s, 1H), 9.4 (s, 1H), 8.9 (s, 1H), 8.25 (s, 1H), 7.78 (d, 1H), 7.70 (d, 1H), 7.54 (d, 1H), 7.48 (d, 1H), 7.40 (t, 2H), 6.56 (d, 1H), 4.02 (s, 2H), 3.82 (s, 3H), 2.80 (s, 6H). MS (EI) m/z for C₂₅H₂₅BrN₆O₄S: 586.79, 584.91 (MH⁺).

Example 77

N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-fluoroethylamino)acetamide. ¹H NMR (400 MHz, DMSO) δ 10.6 (s, 1H), 9.4 (s, 1H), 8.9 (d, 1H), 8.20 (s, 1H), 7.78 (d, 1H), 7.70 (d, 1H), 7.48 (m, 1H), 7.36-7.44 (m, 3H), 7.20 (q, 3H), 6.6 (m, 1H), 4.78 (t, 1H), 4.66 (t, 1H), 3.94 (s, 2H), 3.82 (s, 3H), 3.4 (t, 1H), 3.3 (t, 1H). MS (EI) m/z for C₂₅H₂₄ClFN₆O₄S: 559.2, 561.2 (MH⁺).

Example 78

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)formamide. NMR (400 MHz, DMSO) δ 12.4 (br s, 1H), 10.5 (s, 1H), 8.90 (s, 1H), 8.3 (s, 1H), 7.9 (br s, 1H), 7.85 (d, 1H), 7.75 (d, 1H), 7.5-7.6 (m, 2H), 7.3-7.4 (m, 4H), 6.2 (s, 1H), 3.8 (s, 3H). MS (EI) m/z for C₂₃H₂₁N₅O₅S: 480.1 (MH⁺).

Example 79

N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(3-(dimethylamino)azetidin-1-yl)acetamide. ¹H NMR (400 MHz, DMSO) δ 10.2 (br s, 1H), 9.5 (s, 1H), 8.95 (d, 1H), 8.2 (s, 1H), 7.75 (d, 1H), 7.65 (d, 1H), 7.45 (d, 1H), 7.40 (d, 1H), 7.30-7.35 (t, 1H), 7.1-7.2 (q, 2H), 6.60 (m, 1H), 3.82 (s, 3H). MS (EI) m/z for C₂₈H₃₀ClN₇O₄S: 480.1 (MH⁺).

Example 80

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(pyrrolidin-1-yl)acetamide. MS (EI) m/z for C₂₈H₃₀N₆O₅S: 563.18 (MH⁺).

Example 81

N-(3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(ethyl(methyl)amino)acetamide. NMR (400 MHz, DMSO) δ 12.0 (s, 1H), 10.6 (s, 1H), 9.65 (s, 1H), 9.5 (s, 1H), 8.95 (s, 1H), 8.25 (s, 1H), 7.8 (d, 1H), 7.70 (d, 1H), 7.45-7.50 (d, 1H), 7.3-7.4 (m, 3H), 7.2 (t, 2H), 6.60 (d, 1H), 4.02 (br s, 2H), 3.82 (s, 3H), 3.14 (br s, 2H), 2.80 (s, 3H) 1.2 (t, 3H). MS (EI) m/z for C₂₆H₂₇ClN₆O₄S: 555.2, 557.3 (MH⁺).

Example 82

N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(3-(piperidin-1-yl)azetidin-1-yl)acetamide. MS (EI) m/z for C₃₁H₃₄ClN₇O₄S 2.0×C₂H₁O₂F₃: 636.3, 638.3 (MH⁺).

Example 83

N-(3-(N-(3-(3-fluoro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(methylamino)acetamide. MS (EI) m/z for C₂₄H₂₃FN₆O₄S: 511.04 (MH⁺).

Example 84

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-1-methylpiperidine-4-carboxamide. MS (EI) m/z for C₂₉H₃₂N₆O₅S 1.0×C₂H₄O₂: 577.2 (MH⁺).

Example 85

N-(3-(N-(3-(3-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(methylamino)acetamide. ¹H NMR (400 MHz, DMSO) δ 10.6 (s, 1H), 8.82 (s, 1H), 8.22 (t, 1H), 7.86 (t, 1H), 7.76 (m, 1H), 7.66 (m, 1H), 7.46 (m, 1H), 7.41 (m, 1H), 7.38 (t, 1H), 7.28 (m 1H), 7.24 (t, 1H), 7.12 (m, 2H), 6.56 (d, 1H), 3.88 (s, 2H), 3.80 (s, 3H), 2.60 (s, 3H). MS (EI) m/z for C₂₄H₂₄N₆O₄S: 492.99 (MH⁺).

Example 86

N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2,2,2-trifluoroethylamino)acetamide. ¹H NMR (400 MHz, DMSO) δ 10.4 (s, 1H), 9.2 (s, 1H), 8.65 (s, 1H), 8.4 (s, 1H), 8.00 (m, 1H), 7.80 (d, 1H), 7.75 (d, 1H), 7.65 (q, 1H), 7.55 (t, 1H), 7.40-7.5 (m, 3H), 6.7 (m, 1H), 3.82 (s, 3H), 3.62 (br s, 2H), 3.55 (br d, 2H). MS (EI) m/z for C₂₅H₂₂ClF₃N₆O₄S 1.0×C₂H₁O₂F₃: 595.0, 597.0 (MH⁺).

Example 87

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-(piperidin-1-yl)propanamide. MS (EI) m/z for C₃₀H₃₄N₆O₅S: 591.2 (MH⁺).

Example 88

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-4-(dimethylamino)butanamide. MS (EI) m/z for C₂₈H₃₂N₆O₅S 1.0×C₂H₄O₂: 565.2 (MH⁺).

Example 89

2-(dimethylamino)-N-(3-(N-(3-(3-fluoro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. ¹H NMR (400 MHz, DMSO) δ 10.9 (s, 1H), 9.8 (br s, 1H), 9.1 (s, 1H), 8.34 (s, 1H), 7.90 (d, 1H), 7.76 (d, 1H), 7.52-7.68 (m, 4H), 7.40 (m, 2H), 6.54 (m, 1H), 4.16 (s, 2H), 3.82 (s, 3H), 2.86 (s, 6H). MS (EI) m/z for C₂₅H₂₅FN₆O₄S: 525.05 (MH⁺).

Example 90

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(piperidin-1-yl)acetamide. MS (EI) m/z for C₂₉H₃₂N₆O₅S: 577.37 (MH⁺).

Example 91

2-(dimethylamino)-N-(3-(N-(3-(3-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. ¹H NMR (400 MHz, DMSO) δ 10.5 (s, 1H), 8.8 (s, 1H), 8.25 (s, 1H), 7.83 (t, 1H), 7.76 (d, 1H), 7.64 (d, 1H), 7.3-7.48 (m, 4H), 7.22 (t, 1H), 7.12 (t, 2H), 6.56 (m, 1H), 3.96 (s, 2H), 3.78 (s, 3H), 2.76 (s, 6H). MS (EI) m/z for C₂₅H₂₆N₆O₄S: 507.1 (MH⁺).

Example 92

N-(3-(N-(3-(2-chloro-5-hydroxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(dimethylamino)acetamide. NMR (400 MHz, DMSO) δ 10.8 (s, 1H), 9.9 (s, 1H), 9.8 (s, 1H), 9.1 (s, 1H), 8.55 (s, 1H), 8.34 (s, 1H), 7.9-8.0 (br s, 1H), 7.82 (d, 1H), 7.76 (d, 1H), 7.52-7.66 (m, 2H), 7.42 (t, 1H), 7.26 (d, 1H), 6.50 (m, 1H), 4.16 (s, 2H), 2.86 (s, 6H). MS (EI) m/z for C₂₄H₂₃ClN₆O₄S: 527.1, 529.0 (MH⁺).

Example 93

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-morpholinoacetamide. MS (EI) m/z for C₂₈H₃₀N₆O₆S: 579.1 (MH⁺).

Example 94

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z for C₂₄H₂₃N₅O₅S: 494.0 (MH⁺).

Example 97

2-amino-N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-4-methylphenyl)-2-methylpropanamide. MS (EI) m/z for C₂₆H₂₇ClN₆O₄S: 556.12 (MH⁺).

Example 98

N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(dimethylamino)acetamide. MS (EI) m/z for C₂₅H₂₅ClN₆O₄S: 542.05 (MH⁺).

Example 99

2-amino-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z for C₂₄H₂₄N₆O₅S: 509.59 (MH⁺).

Example 100

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)benzoic acid

To a solution of N-(3-{[2-chloro-5-(methoxy)-phenyl]amino}quinoxalin-2-yl)-3-cyanobenzenesulfonamide (6.02 g, 12.95 mmol), prepared using procedures similar to those in Example 115 or Example 423, in methanol (20 mL) and 1,4-dioxane (20 mL) was added 6.0 N aqueous sodium hydroxide (40 mL) at room temperature. The solution was stirred at 90° C. for 3.5 h. The reaction was cooled to room temperature and neutralized slowly by adding 2.0 N hydrochloric acid until the pH of the solution became in the 2-3 range at 0° C. The solution was diluted with ethyl acetate (300 mL). The organic layer was washed with saturated aqueous sodium chloride (50 mL) and dried over magnesium sulfate. Filtration and concentration at reduced pressure afforded 3-{[(3-{[2-chloro-5-(methoxy)-phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}benzoic acid (5.921 g, 94%). MS (EI) m/z for C₂₂H₁₇ClN₄O₅S: 485.0 (MH⁺).

The following compounds were prepared using procedures similar to those used in Example 100.

Example 101

Proceeding as above, 3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)benzoic acid was prepared. MS (EI) m/z for C₂₃H₂₀N₄O₆S: 481.0 (MH⁺).

Example 102

3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-methyl-1-(piperidin-1-yl)propan-2-yl)benzamide. MS (EI) m/z for C₃₁H₃₅ClN₆O₄S: 623.06 (MH⁺).

Example 103

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-methyl-1-oxo-1-(piperidin-1-yl)propan-2-yl)benzamide. MS (EI) m/z for C₃₁H₃₃ClN₆O₅S: 637.65 (MH⁺).

Example 104

3-{[(3-{[2-chloro-5-(methoxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[2-(dimethylamino)ethyl]benzamide

To a solution of 3-{[(3-{[2-chloro-5-(methoxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}benzoic acid (0.20 g, 0.42 mmol), prepared using procedures similar to Example 100, in dimethylformamide (4 mL) were added 2-(7-aza-1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HATU, 0.32 g, 0.83 mmol) and N-ethyldiisopropylamine (DIEA, 0.13 g, 1.04 mmol) at room temperature. The reaction was stirred for 15 min before N,N-dimethylethane-1,2-diamine (73 mg, 0.83 mmol) was added. The reaction mixture was allowed to stir overnight. The reaction was diluted with ethyl acetate (200 mL) and washed with water (50 mL), saturated aqueous sodium bicarbonate (40 mL), 1.0 N aqueous hydrochloric acid (30 mL), and saturated aqueous sodium chloride (25 mL). The organic layer was dried over magnesium sulfate, filtered and concentrated at reduced pressure to afford 3-{[(3-{[2-chloro-5-(methoxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[2-(dimethylamino)ethyl]benzamide (0.20 g, 87%) as yellow solid. MS (EI) m/z for C₂₆H₂₇ClN₆O₄S: 555.1 (MH⁺).

The following compounds were prepared using procedures similar to those in Example 104.

Example 105

5-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-(dimethylamino)ethyl)-2-methoxybenzamide. ¹H NMR (400 MHz, DMSO-d₆) δ 9.45 (s, 1H), 8.95 (d, 1H), 8.57 (d, 1H), 8.28 (t, 1H), 8.14 (dd, 1H), 7.46 (dd, 1H), 7.39 (m, 2H), 7.17 (m, 4H), 6.60 (dd, 1H), 3.89 (s, 3H), 3.82 (s, 3H), 3.38 (m, 2H), 2.43 (m, 2H), 2.21 (s, 6H). MS (EI) m/z for C₂₇H₂₉ClN₆O₅S: 585.3 (MH⁺).

Example 106

5-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-(dimethylamino)ethyl)-2-fluorobenzamide. ¹H NMR (400 MHz, DMSO-d₆) δ 9.40 (br s, 1H), 9.16 (s, 1H), 8.73 (m, 1H), 8.67 (d, 1H), 8.36 (dd, 1H), 8.26 (m, 1H), 7.94 (br s, 1H), 7.66 (m, 1H), 7.59 (t, 1H), 7.43 (m, 3H), 6.71 (dd, 1H), 3.83 (s, 3H), 3.62 (m, 2H), 3.27 (m, 2H), 2.85 (d, 6H). MS (EI) m/z for C₂₆H₂₆ClFN₆O₄S: 573.1 (MH⁺).

Example 107

3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-(dimethylamino)ethyl)benzamide. MS (EI) m/z for C₂₇H₃₀N₆O₅S: 551.1 (MH⁺).

Example 108

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-(dimethylamino)ethyl)-N-methylbenzamide. MS (EI) m/z for C₂₇H₂₉ClN₆O₄S: 569.1 (MH⁺).

Example 109

3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-(dimethylamino)ethyl)-N-methylbenzamide. MS (EI) m/z for C₂₈H₃₂N₆O₅S: 565.1 (MH⁺).

Example 110 3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)benzamide. MS (EI) m/z for C₂₂H₁₈ClN₅O₄S: 484.0 (MH⁺). Example 111

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-morpholinoethyl)benzamide. MS (EI) m/z for C₂₈H₂₉ClN₆O₅S: 597.0 (MH⁺).

Example 112

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-methylbenzamide. MS (EI) m/z for C₂₃H₂₀ClN₅O₄S: 498.0 (MH⁺).

Example 113

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-morpholinobenzamide. MS (EI) m/z for C₂₆H₂₅ClN₆O₅S: 569.0 (MH⁺).

Example 114

N-(3-{[2-chloro-5-(methoxy)phenyl]amino}quinoxalin-2-yl)-3-{5-[(dimethylamino)methyl]-1,3,4-oxadiazol-2-yl}benzenesulfonamide

To a solution of 3-{[(3-{[2-chloro-5-(methoxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}benzoic acid (0.25 g, 0.52 mmol), prepared as described above in Example 100, in dimethylformamide (2.6 mL) were added 2-(7-aza-1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HATU, 0.25 g, 0.67 mmol) and N-ethyldiisopropylamine (DIEA, 0.11 g, 0.88 mmol) at room temperature. The reaction was stirred for 15 min before 2-(dimethylamino)acetohydrazide (78 mg, 0.67 mmol) was added. The reaction mixture was allowed to stir overnight. The reaction was diluted with ethyl acetate (200 mL) and washed with water (30 mL), saturated aqueous sodium bicarbonate (30 mL), 1.0 N aqueous hydrochloric acid (20 mL), and saturated aqueous sodium chloride (25 mL). The organic layer was dried over magnesium sulfate, filtered and concentrated at reduced pressure to afford 180 mg of a coupled intermediate which was then heated in phosphorus oxychloride (5 mL) at 100° C. for 4 h. The reaction was cooled to room temperature and treated with ice water (50 mL) and extracted with dichloromethane (3×50 mL). The organic layer was dried over magnesium sulfate, filtered and concentrated at reduced pressure to afford a crude product which was subjected to reverse phase HPLC to afford N-(3-{[2-chloro-5-(methoxy)-phenyl]amino}quinoxalin-2-yl)-3-{5-[(dimethylamino)methyl]-1,3,4-oxadiazol-2-yl}-benzenesulfonamide (16 mg, 5%) as yellow solid. MS (EI) m/z for C₂₆H₂₄ClN₇O₄S: 566.0 (MH⁺).

Example 115

N-(3-(3-methoxy-5-nitro-phenylamino)-quinoxalin-2-yl)-3-nitrobenzenesulfonamide

N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide. 2,3-Dichloroquinoxaline (26.1 g, 131.1 mmol), m-Nitrobenzene sulfonamide (26.5 g, 131.1 mmol) and potassium carbonate (18.1 g, 131.1) were dissolved in anhydrous DMSO (500 mL). The reaction was heated to 150° C. for 2 h. The reaction mixture was poured into water (400 mL), followed by addition of 2M HCl (60 mL). The product was extracted with EtOAc (3×500 mL). The organic layers were combined and washed water (2×500 mL) and brine (2×500 mL). The product was then dried with sodium sulfate to give N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide. MS (EI) m/z for C₁₄H₉ClN₄O₄S: 364.94, 366.97 (MH⁺)

N-(3-(3-methoxy-5-nitrophenylamino)quinoxalin-2-yl)-3-nitro-benzenesulfonamide. N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide (700 mg, 1.92 mmol), 3-methoxy-5-nitroaniline (645 mg, 3.84 mmol) and p-xylene (7 mL) were combined and heated to 140° C., then stirred for 16 hours at 130° C. The reaction was allowed to cool, placed in a sep. funnel, diluted with DCM, and washed with 2M HCl and brine and concentrated in vacuo. The resulting solid was washed with Et₂O to give N-(3-(3-methoxy-5-nitro-phenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide (400 mg, 42%). MS (EI) m/z for C₂₁H₁₆N₆O₇S: 496.94 (MH⁺).

The following compounds were prepared using procedures similar to those in Example 115.

Example 116

N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)-3-cyanobenzenesulfonamide. MS (EI) m/z for C₂₂H₁₆ClN₅O₃S: 465.9 (MH⁺).

Example 117 3-cyano-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₃H₁₉N₅O₄S: 462.3 (MH⁺). Example 118

N-(3-(2,5-dimethoxy-phenylamino)quinoxalin-2-yl)-3-fluorobenzenesulfonamide. MS (EI) m/z for C₂₂H₁₉FN₄O₄S: 456.0 (MH⁺).

Example 119

3-bromo-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₂H₁₉BrN₄O₄S: 516.9 (MH⁺).

Example 120

3-bromo-N-(3-(2,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₂H₁₉BrN₄O₄S: 516.9 (MH⁺).

Example 121

N-(3-(3-methoxyphenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₁H₁₈N₄O₃S: 407.0 (MH⁺).

Example 122

N-(3-(4-fluoro-3-methoxyphenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₁H₁₇FN₄O₃S: 425.0 (MH⁺).

Example 123

N-(3-(2,5-dimethoxy-phenylamino)quinoxalin-2-yl)-4-methoxybenzenesulfonamide. MS (EI) m/z for C₂₃H₂₂N₄O₅S: 467.0 (MH⁺).

Example 124

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-4-methoxybenzenesulfonamide. MS (EI) m/z for C₂₃H₂₂N₄O₅S: 467.0 (MH⁺).

Example 125

N-(3-(4-chloro-3-methoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₁H₁₇ClN₄O₃S: 440.9 (MH⁺).

Example 126

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)thiophene-2-sulfonamide. MS (EI) m/z for C₂₀H₁₈N₄O₄S₂: 443.0 (MH⁺).

Example 127

N-(3-(6-methoxyquinolin-8-ylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide. MS (EI) m/z for C₂₄H₁₈N₆O₅S: 502.95 (MH⁺).

Example 128 3-nitro-N-(3-(pyridin-4-ylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₁₉H₁₄N₆O₄S: 423.2 (MH⁺). Example 129

N-(3-(2-chloropyridin-4-ylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide. MS (EI) m/z for C₁₉H₁₃ClN₆O₄S: 456.93, 458.90 (MH⁺).

Example 130

N-(3-(4,6-dimethoxypyrimidin-2-ylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide. MS (EI) m/z for C₂₀H₁₇N₇O₆S: 484.03 (MH⁺).

Example 131

N-(3-(4-hydroxy-6-methoxypyrimidin-2-ylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide. MS (EI) m/z for C₁₉H₁₅N₇O₆S: 469.97 (MH⁺).

Example 132

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-2-fluorobenzenesulfonamide. MS (EI) m/z for C₂₂H₁₉FN₄O₄S: 455.3 (MH⁺).

Example 133

N-(3-(2-bromo-5-methoxy-phenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide. MS (EI) m/z for C₂₁H₁₆BrN₅O₅S: 531.82, 532.84 (MH⁺).

Example 134

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-4-methylbenzenesulfonamide. MS (EI) m/z for C₂₃H₂₂N₄O₄S: 451.0 (MH⁺).

Example 136

N-(3-(2,5-dimethoxy-phenylamino)quinoxalin-2-yl)-4-methylbenzenesulfonamide. MS (EI) m/z for C₂₃H₂₂N₄O₄S: 451.0 (MH⁺).

Example 137

N-(3-(3-fluoro-5-methoxy-phenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide. MS (EI) m/z for C₂₁H₁₆FN₅O₅S: 470.0 (MH⁺).

Example 138

4-bromo-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₂H₁₉BrN₄O₄S: 516.9, 514.9 (MH⁺).

Example 139

N-(3-(3-methoxyphenylamino)quinoxalin-2-yl)-3-nitro-benzenesulfonamide. MS (EI) m/z for C₂₁H₁₇N₅O₅S: 451.93 (MH⁺).

Example 140

N-(3-(2-chloro-5-hydroxy-phenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide. MS (EI) m/z for C₂₀H₁₄ClN₅O₅S: 472.15, 474.13 (MH⁺).

Example 141 3-acetyl-N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₃H₁₉ClN₄O₄S: 483.08 (MH⁺). Example 142

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₂H₂₀N₄O₄S: 437.49 (MH⁺).

Example 143

N-(3-(5-methoxy-2-methyl-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₂H₂₀N₄O₃S: 421.46 (MH⁺).

Example 144

N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₁H₁₇ClN₄O₃S: 440.59 (MH⁺).

Example 145

N-(3-(2,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₂H₂₀N₄O₄S: 437.53 (MH⁺).

Example 146

4-chloro-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₂H₁₉ClN₄O₄S: 470.54 (MH⁺).

Example 147

N-(3-(5-methoxy-2-methyl-phenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide. MS (EI) m/z for C₂₂H₁₉N₅O₅S: 466.32 (MH⁺).

Example 148

N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide. MS (EI) m/z for C₂₁H₁₆ClN₅O₅S: 485.86 (MH⁺).

Example 149

N-(3-(4-chloro-2,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₂H₁₉ClN₄O₄S: 470.99 (MH⁺).

Example 150 N-(3-{[3,5-bis(methoxy)phenyl]amino}quinoxalin-2-yl)-3-(2H-tetrazol-5-yl)benzenesulfonamide

To a stirred solution of 3-cyano-N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)benzenesulfonamide (0.20 g, 0.44 mmol), prepared using procedures similar to those described in Example 115, in dimethylformamide (1.2 mL) at 50° C. were added sodium azide (0.11 g, 1.76 mmol) and ammonium chloride (94 mg, 1.76 mmol). The crude mixture was heated at 100° C. overnight. The reaction was cooled to room temperature treated with ice water (20 mL) followed by concentrated hydrochloric acid (10 mL). The solid obtained was filtered under reduced pressure and washed with hexane (20 mL), diethyl ether (20 mL), and ethyl acetate (5 mL) to afford N-(3-{[3,5-bis(methoxy)phenyl]amino}quinoxalin-2-yl)-3-(2H-tetrazol-5-yl)benzenesulfonamide (55 mg, 25%) as light yellow solid. MS (EI) m/z for C₂₃H₂₀N₈O₄S: 505.0 (MH⁺).

Example 151 N-(3-(2,6-dichloropyridin-4-ylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide

A mixture of N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide (1 g), 2,6-dichloropyridin-4-amine (760 mg) and p-xylene (10 mL) was heated at 135° C. with stirring overnight. Upon cooling to room temperature, the mixture was dissolved in dichloromethane, washed with 2 N HCl (2×) and brine, concentrated in vacuo to give a crude product of N-{3-[(2,6-dichloropyridin-4-yl)amino]quinoxalin-2-yl}-3-nitrobenzenesulfonamide. A small portion of this crude product was purified by HPLC to give N-{3-[(2,6-dichloropyridin-4-yl)amino]quinoxalin-2-yl}-3-nitro-benzenesulfonamide. ¹H NMR (400 MHz, DMSO) δ 9.71 (s, 1H), 8.90 (s, 1H), 8.50 (d, 2H), 8.8.41 (d, 1H), 8.30 (s, 2H), 7.88-7.78 (m, 27.65 (d, 1H), 7.47-7.37 (m, 2H); MS (EI) m/z for C₁₉H₁₂C₁₂N₆O₄S: 491.1, 493.1 (MH⁺).

Example 152 N-(3-(2-chloro-6-methoxypyridin-4-ylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide

To a crude product of N-{3-[(2,6-dichloropyridin-4-yl)amino]quinoxalin-2-yl}-3-nitrobenzenesulfonamide (1.24 g) prepared using procedures similar to those for Example 151, was added anhydrous DMSO (10 mL), followed by sodium methoxide (273 mg). The resulting mixture was heated at 100° C. for 3 days. The mixture was diluted with EtOAc and water, and the pH was adjusted to about 4 by adding acetic acid. The product was extracted with EtOAc (3×). The combined extracts were washed with brine to give the crude product. A portion of the crude product was purified by prep HPLC to give N-(3-{[2-chloro-6-(methyloxy)pyridin-4-yl]amino}quinoxalin-2-yl)-3-nitrobenzenesulfonamide. ¹H NMR (400 MHz, DMSO) δ 9.44 (s, 1H), 8.90 (s, 1H), 8.50 (d, 1H), 8.42 (d, 1H), 7.88-7.84 (m, 2H), 7.77 (s, 1H), 7.74 (s, 1H), 7.64 (d, 1H), 7.45-7.38 (m, 2H), 3.82 (s, 3H); MS (EI) m/z for C₂₀H₁₅ClN₆O₅S: 496.94 (MH⁺).

Example 153 2-(dimethylamino)-N-(3-(N-(3-(3-(2-(dimethylamino)acetamido)-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide

3-amino-N-(3-(3-amino-5-methoxyphenylamino)quinoxalin-2-yl)benzenesulfonamide. N-(3-(3-Methoxy-5-nitrophenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide (400 mg, 0.81 mmol), prepared as described above in Example 115, was dissolved in 1:1 THF:EtOH (4 mL), to which was added formic acid (938 μl, 2.42 mmol) and potassium formate (203 mg, 2.42 mmol). The system was flushed with nitrogen, and then 10% wt Pd/C (50 mg) was added. The reaction was then heated to 60° C. Once the reaction was determined complete by LC-MS, it was allowed to cool, and DMF was added for solubility. The solution was then filtered through a nylon fit to remove the catalyst. The filtrate was diluted water and the pH adjusted to 7 and extracted with DCM (2×) and EtOAc (2×). All organic layers were combined and evaporated to dryness to give 3-amino-N-(3-(3-amino-5-methoxyphenylamino)quinoxalin-2-yl)benzenesulfonamide (330 mg, 93%). MS (EI) m/z for C₂₁H₂₀N₆O₃S: 437.06 (MH⁺)

2-(dimethylamino)-N-(3-(N-(3-(3-(2-(dimethylamino)-acetamido)-5-methoxyphenylamino)quinoxalin-2-yl)-sulfamoyl)phenyl)acetamide. 3-Amino-N-(3-(3-amino-5-methoxyphenylamino)quinoxalin-2-yl)benzenesulfonamide (330 mg, 0.76 mmol), DMF (4 mL), N,N-Dimethylglycine (312 mg, 3.02 mmol), HATU (1.15 g, 3.02 mmol), and 1.29 (mL) (7.56 mmol) DIEA (1.29 mL, 7.56 mmol) were combined and heated to 90° C., followed by heating at 50° C. for over 16 hours. The reaction was allowed to cool, placed into a sep. funnel diluted with water and aqueous LiCl and extracted with EtOAc. The final compound was then purified by prep. HPLC to give 2-(dimethylamino)-N-(3-(N-(3-(3-(2-(dimethylamino)acetamido)-5-methoxy-phenylamino)-quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. ¹H NMR (400 MHz, CD₃OD) δ 8.45 (t, 1H), 7.93 (t, 1H), 7.85-7.88 (m, 1H), 7.70-7.74 (m, 1H), 7.65-7.68 (m, 1H), 7.58-7.62 (m, 1H), 7.58 (t, 1H), 7.34-7.42 (m, 3H), 7.0 (t, 1H), 4.05 (d, 2H), 3.8 (s, 3H), 2.9-3.0 (d, 12H). MS (EI) m/z for C₂₉H₃₄N₈O₅S: 607.2 (MH⁺).

The following title compounds were prepared using procedures similar to those in Example 153.

Example 154

N-(3-(2,5-dimethoxyphenylamino)-7-methylquinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z for C₂₃H₂₂N₄O₄S: 451.0 (MH⁺).

Example 155a and Example 155b N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-3-(methylamino)benzenesulfonamide and N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-3-(dimethylamino)benzenesulfonamide

To a solution of 3-amino-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide (414 mg) in DMF (4.5 mL) was added iodomethane (114 μl). The reaction mixture was heated at 35-50° C. until the formation of both mono-methylated and di-methylated products was detected by LC/MS. The mixture was diluted with EtOAc, washed with water, 10% LiCl (2×) and brine. After removal of solvent in vacuo, the crude mixture was purified by flash silica column chromatography eluting with 15% EtOAc in hexanes, affording the mono-methylated and di-methylated products. Product A: N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-3-(methylamino)-benzenesulfonamide (35 mg). ¹H NMR (400 MHz, DMSO) δ 12.2 (s, 1H), 8.93 (s, 1H), 7.85 (d, 1H), 7.58 (d, 1H), 7.40-7.20 (m, 7H), 6.76 (m, 1H), 6.24 (m, 1H), 6.16 (br s, 1H), 3.77 (s, 6H), 2.71 (s, 3H). MS (EI) for C₂₃H₂₃N₅O₄S: 466.05 (MH+). Product B: N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)-3-(dimethylamino)benzenesulfonamide (33 mg). ¹H NMR (400 MHz, DMSO) δ 1220 (s, 1H), 8.98 (s, 1H), 7.98 (d, 1H), 7.56 (d, 1H), 7.42-7.32 (m, 7H), 6.74 (m, 1H), 6.24 (m, 1H), 3.77 (s, 6H), 2.97 (s, 6H). MS (EI) for C₂₄H₂₅N₅O₄S: 480.04 (MH+).

Example 156 N-(3-{[(2-{[3,5-bis(methoxy)phenyl]amino}pyrido[2,3-b]pyrazin-3-yl)amino]sulfonyl}phenyl)-N-2-[2-(dimethylamino)ethyl]-N-2-methylglycinamide

To a THF suspension (1.3 mL) of 3-amino-N-(3-{[3,5-(dimethoxy)-phenyl]amino}-quinoxalin-2-yl)benzenesulfonamide (126 mg, 0.28 mmol), prepared using procedures similar to those described for Example 15, was added 0.143 mL of 2M aqueous Na₂CO₃. To this yellow suspension is added dropwise 33 μL (0.42 mmol) of chlororacetyl chloride. The reaction mixture turns clear after a few minutes and is allowed to stir at 23° C. for 1 h. To the reaction is added a DMSO (1 mL) solution containing 180 μL (1.4 mmol) of N,N′,N′ trimethylethelyenediamine. The reaction is then warmed to 60° C. and stirred for 18 h. The product is isolated by preparative RP-HPLC (NH₄OAc/ACN) gradient, the appropriate fractions were pooled and lyophilize to give a solid yellow as the acetic acid salt: 59 mg (51%). ¹H-NMR (400 MHz, CDCL₃): δ 10.1 (br s, 1H), 8.37 (br s, 2H), 8.18 (d, 1H), 7.97 (d, 1H), 7.60 (br d, 1H), 7.27 (s, 2H), 7.20 (br s, 3H), 6.15 (s, 1H), 3.82 (m, 2H), 3.65 (s, 6H), 3.20 (br m, 2H), 2.82 (br s, 8H), 2.42 (s, 3H), 2.02 (s, 3H). MS (EI) m/z for C₂₈H₃₄N₈O₅S: 595.84 (MH⁺).

The following title compounds were prepared using similar procedures to those in Example 156.

Example 157

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-((3-(dimethylamino)propyl)(methyl)amino)acetamide. MS (EI) m/z for C₃₀H₃₇N₇O₅S: 608.1 (MH⁺).

Example 158

2-(1,4′-bipiperidin-1′-yl)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z for C₃₄H₄₁N₇O₅S: 660.1 (MH⁺).

Example 159

tert-butyl 2-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenylcarbamoyl)piperidine-1-carboxylate. MS (EI) m/z for C₃₃H₃₈N₆O₇S: 663.1 (MH⁺).

Example 160

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(1-(dimethylamino)propan-2-yl)benzamide. MS (EI) m/z for C₂₇H₂₉ClN₆O₄S: 569.0 (MH⁺).

Example 161

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-3-ureidobenzenesulfonamide. MS (EI) m/z for C₂₃H₂₂N₆O₅S: 495.40 (MH⁺).

Example 162

2-(dimethylamino)-N-(3-(N-(3-(5-methoxy-2-methylphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z for C₂₆H₂₈N₆O₄S: 521.69 (MH⁺).

Example 163

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(4-methylpiperazin-1-yl)acetamide. MS (EI) m/z for C₂₉H₃₃N₇O₅S: 592.61 (MH⁺).

Example 164

2-acetamido-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z for C₂₆H₂₆N₆O₆S: 550.59 (MH⁺).

Example 165

tert-butyl 2-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenylamino)-2-oxoethylcarbamate. MS (EI) m/z for C₂₉H₃₂N₆O₇S: 609.32 (MH⁺).

Example 166 N-(2-(3,5-dimethoxy-phenylamino)pyrido[2,3-b]pyrazin-3-yl)-3-nitrobenzenesulfonamide

To a xylene suspension (15 mL) of N-(2-chloropyrido[2,3-b]pyrazin-3-yl)-3-nitrobenzenesulfonamide (1 g, 2.7 mmol) (prepared using procedures similar to those in Asier, et al J. Org Chem 2005, 70(7), 2878 and Leeson, et al J. Med. Chem. 1991, 34, 1243) was added 420 mg (2.7 mmol) of 3,5 dimethoxyaniline. After refluxing the reaction for 1 h, the reaction is cooled, the precipitate is collected by filtration and dried under vacuum to give 830 mg of the product as a ˜6:1 mixture of isomers with the major being N-(2-(3,5-dimethoxy-phenylamino)pyrido[2,3-b]pyrazin-3-yl)-3-nitrobenzenesulfonamide which was assigned by known chemical reactivity. Analytical HPLC, ret. time=3.3 min (14%), 3.05 min (86%), (conditions: Phenomenex Gemini C18 50×4.6 column, gradient 5% to 95% MeCN/H₂O, in the presence of 0.1% TFA, 5 min run at 3.5 ml/min flow rate, λ=254 nm). ¹H-NMR (400 MHz, DMSO-d6): major isomer δ 9.14 (br s, 1H), 8.69 (dd, 1H), 8.60 (dd, 1H), 8.33 (dt, 2H), 7.77 (t, 1H), 7.49 (dd, 1H), 7.37 d, 2H), 7.05 (s, 1H), 6.26 (t, 1H), 3.77 (s, 6H); MS (EI) m/z for C₂₁H₁₈N₆O₆S: 483.08 (MH⁺).

Example 167 3-amino-N-(2-(3,5-dimethoxy-phenylamino)pyrido[2,3-b]pyrazin-3-yl)benzenesulfonamide

To a 1:1 THF/EtOH suspension (1 mL) of N-(3-(3,5-dimethoxyphenylamino)-pyrido[3,2-b]pyrazin-2-yl)-3-nitrobenzenesulfonamide (190 mg, 0.21 mmol) (prepared using procedures similar to those in Examples 166) was added 47 μL (1.26 mmol) of formic acid plus 99 mg (1.17 mmol) of potassium formate and 50 mg of 10% palladium on charcoal. After refluxing the reaction for 1 h, hot filtration through celite (washing with a small portion of DMF), dilution with 30 mL of water, the pH was adjusted to 5.5 with 5% NaHCO₃, the product is isolated as a precipitate 140 mg (80%) of white powder. Analytical HPLC, ret. time=2.6 min (90%), 3.05 min (10%), 100% pure (conditions: YMC C18 5×4.6 column, gradient 10% to 90% MeCN/H₂O, in the presence of 0.1% TFA, 9 min run at 1 ml/min flow rate, λ=254 nm). ¹H-NMR (400 MHz, CDCL₃): δ 8.48 (br s, 1H), 8.34 (dd, 1H), 7.92 (dd, 1H), 7.41 (dd, 1H), 7.15 (m, 3H), 7.13 (d, 2H), 6.86 (dd, 1H), 6.28 (t, 1H), 3.83 (s, 6H); MS (EI) m/z for C₂₁H₂₀N₆O₄S: 453.03 (MH⁺).

Example 168 3-amino-N-(3-{[3,5-bis(methoxy)phenyl]amino}pyrido[2,3-b]pyrazin-2-yl)benzenesulfonamide

To a 1:1 THF/EtOH suspension (1 mL) of 3-nitro-N-(3-{[3,5-bis(methoxy)-phenyl]amino}pyrido[2,3-b]pyrazin-2-yl)benzenesulfonamide (100 mg, 0.21 mmol) (prepared using procedures similar to those used in Example 166) was added 46 μL (0.63 mmol) of formic acid plus 100 mg (0.63 mmol) of potassium formate and 100 mg of 10% palladium on charcoal. After refluxing the reaction for 1 h, hot filtration through celite, and concentration, the product is isolated by preparative RP-HPLC (NH₄OAc/ACN) gradient. The appropriate fractions were pooled and lyophilize to give solid yellow product: 3.2 mg (4%). ¹H-NMR (400 MHz, CDCl₃): δ 8.62 (d, 1H), 8.52 (s, 1H), 7.62 (d, 1H), 7.3 (m, 4H), 7.18 (d, 2H), 6.88 (d, 1H), 6.27 (t, 1H), 3.96 (br s, 2H), 3.83 (s, 6H). MS (EI) m/z for C₂₁H₂₀N₆O₄S: 453.22 (MH⁺).

Example 169 N-(3-{[2-chloro-5-(methoxy)phenyl]amino}quinoxalin-2-yl)-3-(1-{[2-(dimethylamino)-ethyl]amino}ethyl)benzenesulfonamide trifluoracetic acid salt

To a dichloroethane solution (0.6 mL) of 3-acetyl-N-(3-{[2-chloro-5-(methoxy)-phenyl]amino}quinoxalin-2-yl)benzenesulfonamide (150 mg, 0.31 mmol), prepared using procedures similar to those in Example 115, and 51 μL (0.37 mmol) of N,N-dimethylethylenediamine was added 19 μL of acetic acid followed by 132 mg (0.62 mmol) of sodium cyanoborohydride. The reaction mixture was refluxed for 18 h under a nitrogen atmosphere. After concentration (in vacuo), the product is isolated by preparative RP-HPLC (0.1% TFA/ACN) gradient, followed by lyophilization of appropriate fractions to give solid yellow solid: 189 mg (90%). ¹H-NMR (400 MHz, d₃-MeOD): δ 8.74 (s, 1H), 8.18 (s, 1H), 8.12 (d, 1H), 7.71 (m, 3H), 7.48 (m, 4H), 7.28 (d, 1H), 6.63 (d, 1H), 4.38 (q, 1H), 3.80 (s, 3H), 3.30 (m, 3H), 3.12 (m, 1H), 2.84 (s, 3H), 1.60 (d, 3H). MS (EI) m/z for C₂₇H₃₁ClN₆O₃S: 555.56 (MH⁺).

Example 170 N,N-{[(3-{[(3-{[2-chloro-5-(methoxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-4-methylphenyl)amino](dimethylamino)methylidene}-N-methylmethanaminium

To a dimethylformamide solution (1 mL) of 3-amino-N-(3-{[2-chloro-5-(methoxy)-phenyl]amino}quinoxalin-2-yl)2-methylbenzenesulfonamide (200 mg, 0.40 mmol), prepared using procedures similar to those described in Example 115, is added 312 μL (1.8 mmol) of DIEA and 122 mg (0.6 mmol) of HATU. After stirring for 18 h at 60° C., the product was precipitated from a 1:1 mixture of hexane/ethyl acetate, filtered and dried to afford 60 mg (26%). ¹H NMR (400 MHz, DMSO-d₆): δ 9.26 (b rs, 1H), 8.96 (br s, 1H), 7.80 (s, 1H), 7.51 (br s, 1H), 7.45 (d, 1H), 7.18 (brm, 4H), 6.91 (br s, 1H), 6.60 (br d, 1H), 3.82 (s, 3H), 3.36 (s, 3H), 2.85 (s, 6H), 2.58 (s, 3H). MS (EI) m/z for C₂₇H₃₁ClN₇O₃S⁺: 569.32 (MH⁺).

Example 171 2-Bromo-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide

In a 50 mL round-bottom flask was added 2-bromoacetic acid (1.87 g, 13.5 mmol), N,N-diisopropylcarbodiimide (860 mg, 6.8 mmol) and 10 mL DCM. To this mixture was added 3-amino-N-(3-(3,5-dimethoxyphenylamino) quinoxalin-2-yl)benzenesulfonamide (2.03 g, 4.5 mmol), prepared using procedures similar to those in Example 168. The reaction was stirred overnight at room temperature. Complete consumption of the starting aniline was confirmed by LCMS. The solvent was evaporated off to yield the crude product (2-bromo-N-(3-(N-(3-(3,5-dimethoxyphenylamino) quinoxalin-2-yl)sulfamoyl)phenyl)acetamide). This was used directly in the next step without further purification.

General Alkylation Procedure 1

Into a 2-dram vial was placed 2-bromo-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl) sulfamoyl)phenyl)acetamide (86 mg, 0.15 mmol), prepared using procedures similar to those in Example 171,along with 2 mL of acetonitrile. Eight equivalents (1.2 mmol) of the desired amine, aniline, hydrazine or alkoxyamine were added followed by the addition of Hunig's Base (41 μL, 0.25 mmol). The reaction then was stirred at 50° C. for one hour (overnight for aniline reagents). Preparative reverse-phase HPLC was used to isolate the desired product directly from the crude reaction mixture. A Waters Fractionlynx preparative reverse-phase HPLC—equipped with a Waters SunFire Prep C18, OCD 5 μM, 30×70 mm column and running a 5-100% gradient with a binary solvent system of 25 mM ammonium acetate in water/acetonitrile—was used to carry out the purification.

The following title compounds were prepared according to General Library Alkylation Procedure 1.

Example 172

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(methylamino)acetamide. ¹H-NMR (400 MHz, d₆-DMSO): 8.81 (s, 1H), 8.23 (t, 1H), 7.75 (d, 1H), 7.66 (d, 1H), 7.41-7.38 (m, 1H), 7.35 (m, 1H), 7.32 (d, 2H), 7.29-7.27 (m, 1H), 7.14-7.11 (m, 2H), 6.14 (t, 1H), 3.80 (s, 1H), 3.78 (s, 6H), 2.58 (s, 3H), 1.91 (s, 2H); MS (EI) m/z C₂₅H₂₆N₆O₅S: 523.6 (MH⁺).

Example 173 2-(cyclopropylmethylamino)-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. ¹H-NMR (400 MHz, d₆-DMSO): 10.58 (s, 1H), 8.81 (s, 1H), 8.20 (t, 1H), 7.76 (d, 1H), 7.67 (d, 1H), 7.42-7.36 (m, 2H), 7.32 (d, 2H), 7.27 (s, 1H), 7.14-7.12 (m, 2H), 6.15 (t, 1H), 3.93 (s, 2H), 3.78 (s, 6H), 2.89 (s, 1H), 2.88 (s, 1H), 1.05-1.00 (m, 1H), 0.59 (d, 1H), 0.57 (d, 1H), 0.35 (d, 1H), 0.34 (d, 1H); MS (EI) m/z C₂₈H₃₀N₆O₅S: 563.6 (MH⁺). Example 174

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-hydroxy-propylamino)acetamide. ¹H-NMR (400 MHz, d₆-DMSO): 10.49 ppm (s, 1H), 8.81 ppm (s, 1H), 8.23 ppm (t, 1H), 8.13 ppm (s, 1H), 7.76 ppm (d, 1H), 7.765-7.763 (dd, 1H), 7.41-7.37 ppm (m, 2H), 7.33-7.32 ppm (d, 1H), 7.30-7.28 ppm (m, 1H), 7.16-7.09 ppm (m, 2H), 6.55 ppm (s, 1H), 6.14 ppm (t, 1H), 5.49 ppm (d, 2H), 5.25 ppm (s, 1H), 3.85 ppm (s, 1H), 3.78 ppm (s, 6H) 3.67-3.59 ppm (m, 1H), 3.00-2.89 ppm (dd, 1H), 2.79-2.76 ppm (m, 1H), 1.10 ppm (d, 1H), 1.01-0.99 ppm (d, 1H); MS (EI) m/z C₂₇H₃₀N₆O₆S: 566.6 (MH⁺).

Example 175

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(3-fluorobenzylamino)acetamide. ¹H-NMR (400 MHz, d₆-DMSO): 10.42 ppm (s, 1H), 8.82 ppm (s, 1H), 8.23 ppm (s, 1H), 8.14 ppm (s, 1H), 7.75 ppm (d, 1H), 7.65 ppm (d, 1H), 7.49-7.32 ppm (m, 6H), 7.25-7.20 ppm (m, 1H), 7.14-7.12 ppm (m, 2H), 6.55 ppm (s, 1H), 6.15 ppm (t, 1H), 4.14 ppm (s, 2H), 3.78 ppm (s, 6H), 3.74 ppm (s, 2H); MS (EI) m/z C₃₁H₂₉FN₆O₅S: 616.7 (MH⁺).

Example 176

2-(benzylamino)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₁H₃₀N₆O₅S: 599 (MH⁺).

Example 177

2-(diethylamino)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₂₈H₃₂N₆O₅S: 565 (MH⁺).

Example 178

2-(4-(3,4-dichlorophenyl)piperazin-1-yl)-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₄H₃₃Cl₂N₇O₅S: 722 (MH⁺).

Example 179

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2,2-dimethylhydrazinyl)acetamide. MS (EI) m/z C₂₆H₂₉N₇O₅S: 552 (MH⁺).

Example 180

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(p-tolylamino)acetamide. MS (EI) m/z C₃₁H₃₀N₆O₅S: 599 (MH⁺).

Example 181

2-(benzyloxyamino)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₁H₃₀N₆O₆S: 615 (MH⁺).

Example 182

2-(2-chlorophenylamino)-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₀H₂₇ClN₆O₅S: 619 (MH⁺).

Example 183

N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(isopropylamino)acetamide. MS (EI) m/z C₂₇H₃₀N₆O₅S: 551 (MH⁺).

Example 184

2-(4-cyclopentylpiperazin-1-yl)-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₃H₃₉N₇O₅S: 646 (MH⁺).

Example 185

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(4-propylpiperidin-1-yl)acetamide. MS (EI) m/z C₃₂H₃₈N₆O₅S: 619 (MH⁺).

Example 186

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(isobutoxyamino)acetamide. MS (EI) m/z C₂₈H₃₂N₆O₆S: 581 (MH⁺).

Example 187

2-(3-tert-butylphenylamino)-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₄H₃₆N₆O₅S: 641 (MH⁺).

Example 188

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-phenylpropan-2-ylamino)acetamide. MS (EI) m/z C₃₃H₃₄N₆O₅S: 627 (MH⁺).

Example 189

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(3-fluoro-4-hydroxyphenylamino)acetamide. MS (EI) m/z C₃₀H₂₇FN₆O₆S: 619 (MH⁺).

Example 190

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-(methylthio)benzylamino)acetamide. MS (EI) m/z C₃₂H₃₂N₆O₅S₂: 645 (MH⁺).

Example 191

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(5-fluoro-2-methylbenzylamino)acetamide. MS (EI) C₃₂H₃₁FN₆O₅S: 631 (MH⁺).

Example 192

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-phenylpyrrolidin-1-yl)acetamide. MS (EI) m/z C₃₄H₃₄N₆O₅S: 639 (MH⁺).

Example 193

2-(2-benzylpyrrolidin-1-yl)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₅H₃₆N₆O₅S: 653 (MH⁺).

Example 194

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-phenylmorpholino)acetamide. MS (EI) m/z C₃₄H₃₄N₆O₆S: 655 (MH⁺).

Example 195

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-(pyridin-4-yl)piperidin-1-yl)acetamide. MS (EI) m/z C₃₄H₃₅N₇O₅S: 654 (MH⁺).

Example 196

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(o-tolylamino)acetamide. MS (EI) m/z C₃₁H₃₀N₆O₅S: 599 (MH⁺).

Example 197

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2,4-dimethylbenzylamino)acetamide. MS (EI) m/z

C₃₃H₃₄N₆O₅S: 627 (MH⁺).

Example 198

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(methyl(pyridin-3-ylmethyl)amino)acetamide. MS (EI) m/z C₃₁H₃₁N₇O₅S: 614 (MH⁺).

Example 199

2-(3-chloro-4-methylbenzylamino)-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₂H₃₁ClN₆O₅S: 647 (MH⁺).

Example 200

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-((2-(dimethylamino)-ethyl)(methyl)amino)acetamide. MS (EI) m/z C₂₉H₃₅N₇O₅S: 594 (MH⁺).

Example 201

2-(4-acetylpiperazin-1-yl)-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₀H₃₃N₇O₆S: 620 (MH⁺).

Example 202

N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(methyl(1-methylpyrrolidin-3-yl)amino)acetamide. MS (EI) m/z C₃₀H₃₅N₇O₅S: 606 (MH⁺).

Example 203

N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(4-methyl-1,4-diazepan-1-yl)acetamide. MS (EI) m/z C₃₀H₃₅N₇O₅S: 606 (MH⁺).

Example 204

2-(4-allylpiperazin-1-yl)-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₁H₃₅N₇O₅S: 618 (MH⁺).

Example 205

N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(4-isopropylpiperazin-1-yl)acetamide MS (EI) m/z C₃₁H₃₇N₇O₅S: 620 (MH⁺).

Example 206

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(3-(dimethylamino)pyrrolidin-1-yl)acetamide. MS (EI) m/z C₃₀H₃₅N₇O₅S: 606 (MH⁺).

Example 207

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(3-(dimethylamino)azetidin-1-yl)acetamide. MS (EI) m/z C₂₉H₃₃N₇O₅S: 592 (MH⁺).

Example 208

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(4-oxopiperidin-1-yl)acetamide. MS (EI) m/z C₂₉H₃₀N₆O₆S: 591 (MH⁺).

Example 209

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-((2-methoxyethyl)(methyl)amino)acetamide. MS (EI) m/z C₂₈H₃₂N₆O₆S: 581 (MH⁺).

Example 210

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(4-methylbenzyloxyamino)acetamide. MS (EI) m/z C₃₂H₃₂N₆O₆S: 629 (MH⁺).

Example 211

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-methoxybenzyloxyamino)acetamide. MS (EI) m/z C₃₂H₃₂N₆O₇S: 645 (MH⁺).

Example 212

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(propylamino)acetamide. MS (EI) m/z C₂₇H₃₀N₆O₅S: 551 (MH⁺).

Example 213

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(ethyl(methyl)amino)acetamide. MS (EI) m/z C₂₇H₃₀N₆O₅S: 551 (MH⁺).

Example 214

2-(allyl(methyl)amino)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₂₈H₃₀N₆O₅S: 563 (MH⁺).

Example 215 2-(tert-butylamino)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₂₈H₃₂N₆O₅S: 565 (MH⁺). Example 216

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(isobutylamino)acetamide. MS (EI) m/z C₂₈H₃₂N₆O₅S: 565 (MH⁺).

Example 217 2-(butylamino)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₂₈H₃₂N₆O₅S: 565 (MH⁺). Example 218

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(isopropyl(methyl)amino)acetamide. MS (EI) m/z C₂₈H₃₂N₆O₅S: 565 (MH⁺).

Example 219

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(4-formylpiperazin-1-yl)acetamide. MS (EI) m/z C₂₉H₃₁N₇O₆S: 606 (MH⁺).

Example 220

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(4-ethylpiperazin-1-yl)acetamide. MS (EI) m/z C₃₀H₃₅N₇O₅S: 606 (MH⁺).

Example 221

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(4-formyl-1,4-diazepan-1-yl)acetamide. MS (EI) m/z C₃₀H₃₃N₇O₆S: 620 (MH⁺).

Example 222

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(ethyl(2-hydroxyethyl)amino)acetamide. MS (EI) m/z C₂₈H₃₂N₆O₆S: 581 (MH⁺).

Example 223

(S)—N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(3-hydroxypyrrolidin-1-yl)acetamide. MS (EI) m/z C₂₈H₃₀N₆O₆S: 579 (MH⁺).

Example 224

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2,6-dimethylmorpholino)acetamide. MS (EI) m/z C₃₀H₃₄N₆O₆S: 607 (MH⁺).

Example 225

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxatin-2-yl)sulfamoyl)phenyl)-2-(2-methylbenzylamino)acetamide. MS (EI) m/z C₃₂H₃₂N₆O₅S: 613 (MH⁺).

Example 226

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-methoxy-ethylamino)acetamide. MS (EI) m/z C₂₇H₃₀N₆O₆S: 567 (MH⁺).

Example 227

N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(thiazolidin-3-yl)acetamide. MS (EI) m/z C₂₇H₂₈N₆O₅S₂: 581 (MH⁺).

Example 228

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(3-(hydroxymethyl)piperidin-1-yl)acetamide. MS (EI) m/z C₃₀H₃₄N₆O₆S: 607 (MH⁺).

Example 229

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-phenylpropylamino)acetamide. MS (EI) m/z C₃₃H₃₄N₆O₅S: 627 (MH⁺).

Example 230

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(isobutyl(methyl)amino)acetamide. MS (EI) m/z C₂₉H₃₄N₆O₅S: 579 (MH⁺).

Example 231

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(phenylamino)acetamide. MS (EI) m/z C₃₀H₂₈N₆O₅S: 585 (MH⁺).

Example 232

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-propylphenylamino)acetamide. MS (EI) m/z C₃₃H₃₄N₆O₅S: 627 (MH⁺).

Example 233

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-isopropylphenylamino)acetamide. MS (EI) m/z C₃₃H₃₄N₆O₅S: 627 (MH⁺).

Example 234

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-fluoro-4-methylphenylamino)acetamide. MS (EI) m/z C₃₁H₂₉FN₆O₅S: 617 (MH⁺).

Example 235 2-(4-chlorophenylamino)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₀H₂₇ClN₆O₅S: 619 (MH⁺). Example 236

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-methoxyphenylamino)acetamide. MS (EI) m/z C₃₁H₃₀N₆O₆S: 615 (MH⁺).

Example 237

2-(3-chlorophenylamino)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₀H₂₇ClN₆O₅S: 619 (MH⁺).

Example 238

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2,3-dimethylphenylamino)acetamide. MS (EI) m/z C₃₂H₃₂N₆O₅S: 613 (MH⁺).

Example 239

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-fluorophenylamino)acetamide. MS (EI) m/z C₃₀H₂₇FN₆O₅S: 603 (MH⁺).

Example 240

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(3-fluorophenylamino)acetamide. MS (EI) m/z C₃₀H₂₇FN₆O₅S: 603 (MH⁺).

Example 241

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(thiophen-2-ylmethylamino)acetamide. MS (EI) m/z C₂₉H₂₈N₆O₅S₂: 605 (MH⁺).

Example 242

2-(cyclohexyl(ethyl)amino)-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₂H₃₈N₆O₅S: 619 (MH⁺).

Example 243

2-((cyclopropylmethyl)(propyl)amino)-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₁H₃₆N₆O₅S: 605 (MH⁺).

Example 244

2-(allyl(cyclopentyl)amino)-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₂H₃₆N₆O₅S: 617 (MH⁺).

Example 245

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(ethyl(isopropyl)amino)acetamide. MS (EI) m/z C₂₉H₃₄N₆O₅S: 579 (MH⁺).

Example 246

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(ethyl(phenyl)amino)acetamide. MS (EI) m/z C₃₂H₃₂N₆O₅S: 613 (MH⁺).

Example 247

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-methylpyrrolidin-1-yl)acetamide. MS (EI) m/z C₂₉H₃₂N₆O₅S: 577 (MH⁺).

Example 248

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-methylpiperidin-1-yl)acetamide. MS (EI) m/z C₃₀H₃₄N₆O₅S: 591 (MH⁺).

Example 249

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(pyridin-2-ylmethylamino)acetamide. MS (EI) m/z C₃₀H₂₉N₇O₅S: 600 (MH⁺).

Example 250

2-(benzyl(methyl)amino)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₂H₃₂N₆O₅S: 613 (MH⁺).

Example 251

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(1-phenylethylamino)acetamide. MS (EI) m/z C₃₂H₃₂N₆O₅S: 613 (MH⁺).

Example 252

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(3-methylpiperidin-1-yl)acetamide. MS (EI) m/z C₃₀H₃₄N₆O₅S: 591 (MH⁺).

Example 253

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(4-methylpiperidin-1-yl)acetamide. MS (EI) m/z C₃₀H₃₄N₆O₅S: 591 (MH⁺).

Example 254

2-(3,4-dihydroisoquinolin-2(1H)-yl)-N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₃H₃₂N₆O₅S: 625 (MH⁺).

Example 255

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2,6-dimethylpiperidin-1-yl)acetamide. MS (EI) m/z C₃₁H₃₆N₆O₅S: 605 (MH⁺).

Example 256

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(3-hydroxybenzylamino)acetamide. MS (EI) m/z C₃₁H₃₀N₆O₆S: 615 (MH⁺).

General Library Acylation Procedure 1

Into a 2-dram vial were added 3-amino-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide (54 mg, 0.12 mmol), prepared using procedures similar to those described in Example 15, DMA (2 mL) and the desired carboxylic acid (0.17 mmol). DIEA (70 μL, 0.4 mmol) followed by HATU (53 mg, 0.14 mmol) were added to the vial and the reaction mixture stirred at 50° C. overnight. Preparative reverse-phase HPLC was used to isolate the desired product directly from the crude reaction mixture. A Waters Fractionlynx preparative reverse-phase HPLC; equipped with a Waters SunFire Prep C18, OCD 5 μM, 30×70 mm column and running a 5-100% gradient with a binary solvent system of 25 mM ammonium acetate in water/acetonitrile; was used to carry out the purification.

The following title compounds were prepared according to General Library Acylation Procedure 1.

Example 257

N-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)morpholine-4-carboxamide: MS (EI) m/z for C₂₆H₂₅ClN₆O₅S: 567 (MH⁻).

Example 258

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(dimethylamino)acetamide. MS (EI) m/z for C₂₆H₂₈N₆O₅S: 535.1 (MH⁻).

Example 259

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)propionamide. ¹H-NMR (400 MHz, d₆-DMSO): 12.37 (s, 1H), 10.20 (s, 1H), 8.88 (s, 1H), 8.37 (s, 1H), 7.93 (s, 1H), 7.77 (t, 2H), 7.59 (t, 1H), 7.51 (t, 1H), 7.41-7.34 (m, 4H), 6.24 (t, 1H), 3.76 (s, 6H), 2.36-2.31 (dd, 2H), 1.10 (s, 1H), 1.08 (s, 1H), 1.06 (s, 1H); MS (EI) m/z C₂₅H₂₅N₅O₅S: 508.6 (MH⁺).

Example 260

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)Phenyl)pyridazine-4-carboxamide. ¹H-NMR (400 MHz, d₆-DMSO): 11.01 (s, 1H), 9.66 (dd, 1H), 9.52 (dd, 1H), 8.90 (s, 1H), 8.55 (s, 1H), 8.13 (dd, 1H), 7.99 (d, 1H), 7.93 (d, 1H), 7.65-7.58 (m, 2H), 7.42-7.35 (m, 4H), 6.24 (t, 1H), 3.75 (s, 6H); MS (EI) m/z C₂₇H₂₃N₇O₅S: 558.6 (MH⁺).

Example 261

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-methylnicotinamide. ¹H-NMR (400 MHz, d₆-DMSO): 10.78 ppm (s, 1H), 8.90 ppm (s, 1H), 8.58-8.57 ppm (dd, 2H), 7.90-7.86 (m, 4H), 7.60-7.56 ppm (m, 2H), 7.42-7.34 (m, 5H), 6.23 ppm (t, 1H), 3.74 ppm (s, 6H), 2.57 ppm (s, 3H); MS (EI) m/z C₂₉H₂₆N₅O₅S: 570.6 (MH⁺).

Example 262

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(o-tolyloxy)acetamide. ¹H-NMR (400 MHz, d₆-DMSO): 12.37 ppm (s, 1H), 10.41 ppm (s, 1H), 8.90 ppm (s, 1H), 8.41 ppm (s, 1H), 7.93 ppm (s, 1H), 7.90-7.8 (m, 2H), 7.59-7.53 ppm (m, 2H), 7.42-7.33 ppm (m, 4H), 7.17-7.12 ppm (m, 2H), 6.89-6.85 ppm (m, 2H), 6.24 ppm (t, 1H), 4.74 ppm (s, 2H), 3.76 ppm (s, 6H), 2.33 ppm (s, 2H); MS (EI) m/z C₃₁H₂₉N₅O₆S: 599.7 (MH⁺).

Example 263

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-methoxy-4-methylbenzamide. MS (EI) m/z C₃₁H₂₉N₅O₆S: 600 (MH⁺).

Example 264

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-methoxy-4-methylbenzamide. MS (EI) m/z C₂₈H₂₄N₆O₅S: 557 (MH⁺).

Example 265

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)thiazole-4-carboxamide. MS (EI) m/z C₂₆H₂₂N₆O₅S₂: 563 (MH⁺).

Example 266

2-bromo-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)thiophene-3-carboxamide. MS (EI) m/z C₂₇H₂₂BrN₅O₅S₂ 640 (MH⁺).

Example 267

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)pivalamide. MS (EI) m/z C₂₇H₂₉N₅O₅S: 536 (MH⁺).

Example 268

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)pent-4-enamide. MS (EI) m/z C₂₇H₂₇N₅O₅S: 534 (MH⁺).

Example 269

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)benzamide. MS (EI) m/z C₂₉H₂₅N₅O₅S: 556 (MH⁺).

Example 270

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)butyramide. MS (EI) m/z C₂₆H₂₇N₅O₅S: 522 (MH⁺).

Example 271

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-methoxyacetamide. MS (EI) m/z C₂₅H₂₅N₅O₆S: 524 (MH⁺).

Example 272

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)cyclobutanecarboxamide. MS (EI) m/z C₂₇H₂₇N₅O₅S: 534 (MH⁺).

Example 273

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-methylcyclopropanecarboxamide. MS (EI) m/z C₂₇H₂₇N₅O₅S: 534 (MH⁺).

Example 274

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-1-methylcyclopropanecarboxamide. MS (EI) m/z C₂₇H₂₇N₅O₅S: 534 (MH⁺).

Example 275

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-methylbutanamide. MS (EI) m/z C₂₇H₂₉N₅O₅S: 536 (MH⁺).

Example 276

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-ethoxyacetamide. MS (EI) m/z C₂₆H₂₇N₅O₆S: 538 (MH⁺).

Example 277

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-methoxypropanamide. MS (EI) m/z C₂₆H₂₇N₅O₆S: 538 (MH⁺).

Example 278

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-hydroxyacetamide. MS (EI) m/z C₂₄H₂₃N₅O₆S: 510 (MH⁺).

Example 279

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)isobutyramide. MS (EI) m/z C₂₆H₂₇N₅O₅S: 522 (MH⁺).

Example 280

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-1-hydroxycyclopropanecarboxamide. MS (EI) m/z C₂₆H₂₅N₅O₆S: 536 (MH⁺).

Example 281

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)furan-3-carboxamide. MS (EI) m/z C₂₇H₂₃N₅O₆S: 546 (MH⁺).

Example 282

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)tetrahydrofuran-3-carboxamide. MS (EI) m/z C₂₇H₂₇N₅O₆S: 550 (MH⁺).

Example 283

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)tetrahydrofuran-2-carboxamide. MS (EI) m/z C₂₇H₂₇N₅O₆S: 550 (MH⁺).

Example 284

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)furan-2-carboxamide. MS (EI) m/z C₂₇H₂₃N₅O₆S: 546 (MH⁺).

Example 285

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)isonicotinamide. MS (EI) m/z C₂₈H₂₄N₆O₅S: 557 (MH⁺).

Example 286

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-1H-pyrrole-2-carboxamide. MS (EI) m/z C₂₇H₂₄N₆O₅S: 545 (MH⁺).

Example 287

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)pyrazine-2-carboxamide. MS (EI) m/z C₂₇H₂₃N₇O₅S: 558 (MH⁺).

Example 288

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-1-methyl-1H-pyrrole-2-carboxamide. MS (EI) m/z C₂₈H₂₆N₆O₅S: 559 (MH⁺).

Example 289

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-5-methylisoxazole-3-carboxamide. MS (EI) m/z C₂₇H₂₄N₆O₆S: 561 (MH⁺).

Example 290

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)thiophene-2-carboxamide. MS (EI) m/z C₂₇H₂₃N₅O₅S₂: 562 (MH⁺).

Example 291

(S)—N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-1-methylpyrrolidine-2-carboxamide. MS (EI) m/z C₂₈H₃₀N₆O₅S: 563 (MH⁺).

Example 292

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-methylbenzamide. MS (EI) m/z C₃₀H₂₇N₅O₅S: 570 (MH⁺).

Example 293

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-phenylacetamide. MS (EI) m/z C₃₀H₂₇N₅O₅S: 570 (MH⁺).

Example 294

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-methylpicolinamide. MS (EI) m/z C₂₉H₂₆N₆O₅S: 571 (MH⁺).

Example 295

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(pyridin-3-yl)acetamide. MS (EI) m/z C₂₉H₂₆N₆O₅S: 571 (MH⁺).

Example 296

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-6-hydroxypicolinamide. MS (EI) m/z C₂₈H₂₄N₆O₆S: 573 (MH⁺).

Example 297

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-fluorobenzamide MS (EI) m/z C₂₉H₂₄FN₅O₅S: 574 (MH⁺).

Example 298

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-4-fluorobenzamide. MS (EI) m/z C₂₉H₂₄FN₅O₅S: 574 (MH⁺).

Example 299

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-fluorobenzamide. MS (EI) m/z C₂₉H₂₄FN₅O₅S: 574 (MH⁺).

Example 300

2-cyclohexyl-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₀H₃₃N₅O₅S: 576 (MH⁺).

Example 301

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-oxocyclopentyl)acetamide. MS (EI) m/z C₂₉H₂₉N₅O₆S: 576 (MH⁺).

Example 302

4-cyclopropyl-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-4-oxobutanamide. MS (EI) m/z C₂₉H₂₉N₅O₆S: 576 (MH⁺).

Example 303

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-oxocyclohexanecarboxamide. MS (EI) m/z C₂₉H₂₉N₅O₆S: 576 (MH⁺).

Example 304

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-(pyridin-3-yl)propanamide. MS (EI) m/z C₃₀H₂₈N₆O₅S: 585 (MH⁺).

Example 305

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-methoxybenzamide. MS (EI) m/z C₃₀H₂₇N₅O₆S: 586 (MH⁺).

Example 306

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-methoxybenzamide. MS (EI) m/z C₃₀H₂₇N₅O₆S: 586 (MH⁺).

Example 307

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-phenoxyacetamide. MS (EI) m/z C₃₀H₂₇N₅O₆S: 586 (MH⁺).

Example 308

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-4-methoxybenzamide. MS (EI) m/z C₃₀H₂₇N₅O₆S: 586 (MH⁺).

Example 309

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(4-fluorophenyl)acetamide. MS (EI) m/z C₃₀H₂₆FN₅O₅S: 588 (MH⁺).

Example 310

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-fluorophenyl)acetamide. MS (EI) m/z C₃₀H₂₆FN₅O₅S: 588 (MH⁺).

Example 311

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(3-fluorophenyl)acetamide. MS (EI) m/z C₃₀H₂₆FN₅O₅S: 588 (MH⁺).

Example 312

2-chloro-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)benzamide. MS (EI) m/z C₂₉H₂₄ClN₅O₅S: 590 (MH⁺).

Example 313

4-chloro-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)benzamide. MS (EI) m/z C₂₉H₂₄ClN₅O₅S: 590 (MH⁺).

Example 314

3-chloro-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)benzamide. MS (EI) m/z C₂₉H₂₄ClN₅O₅S: 590 (MH⁺).

Example 315

(1R,2R)—N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-phenylcyclopropanecarboxamide. MS (EI) m/z C₃₂H₂₉N₅O₅S: 596 (MH⁺).

Example 316

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-1-phenylcyclopropanecarboxamide. MS (EI) m/z C₃₂H₂₉N₅O₅S: 596 (MH⁺).

Example 317

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(1H-imidazol-4-yl)acetamide. MS (EI) m/z C₂₇H₂₅N₇O₅S: 560 (MH⁺).

Example 318

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-4-methoxy-2-methylbenzamide. MS (EI) m/z C₃₁H₂₉N₅O₆S: 600 (MH⁺).

Example 319

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(4-fluorophenoxy)acetamide. MS (EI) m/z C₃₀H₂₆FN₅O₆S: 604 (MH⁺).

Example 320

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-5-fluoro-2-methoxybenzamide. MS (EI) m/z C₃₀H₂₆FN₅O₆S: 604 (MH⁺).

Example 321

2-(4-chlorophenyl)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₀H₂₆ClN₅O₅S: 604 (MH⁺).

Example 322

2-(2-chlorophenyl)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₀H₂₆ClN₅O₅S: 604 (MH⁺).

Example 323

2-(3-chlorophenyl)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₃₀H₂₆ClN₅O₅S: 604 (MH⁺).

Example 324

1-acetyl-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)piperidine-4-carboxamide. MS (EI) m/z C₃₀H₃₂N₆O₆S: 605 (MH⁺).

Example 325

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(pyridin-4-yl)acetamide. MS (EI) m/z C₂₉H₂₆N₆O₅S: 571 (MH⁺).

Example 326

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(pyridin-2-yl)acetamide. MS (EI) m/z C₂₉H₂₆N₆O₅S: 571 (MH⁺).

Example 327

2,4-dichloro-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)benzamide. MS (EI) m/z C₂₉H₂₃Cl₂N₅O₅S: 624 (MH⁺).

Example 328

3,4-dichloro-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)benzamide. MS (EI) m/z C₂₉H₂₃Cl₂N₅O₅S: 624 (MH⁺).

Example 329

2,5-dichloro-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)benzamide. MS (EI) m/z C₂₉H₂₃Cl₂N₅O₅S: 624 (MH⁺).

Example 330

3,5-dichloro-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)benzamide. MS (EI) m/z C₂₉H₂₃Cl₂N₅O₅S: 624 (MH⁺).

Example 331

2,3-dichloro-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)benzamide. MS (EI) m/z C₂₉H₂₃Cl₂N₅O₅S: 624 (MH⁺).

Example 332

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)pentanamide. MS (EI) m/z C₂₇H₂₉N₅O₅S: 536 (MH⁺).

Example 333

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-methylbutanamide. MS (EI) m/z C₂₇H₂₉N₅O₅S: 536 (MH⁺).

Example 334

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-1H-imidazole-2-carboxamide. MS (EI) m/z C₂₆H₂₃N₇O₅S: 546 (MH⁺).

Example 335

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-1H-imidazole-4-carboxamide. MS (EI) m/z C₂₆H₂₃N₇O₅S: 546 (MH⁺).

Example 336

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)isoxazole-5-carboxamide. MS (EI) m/z C₂₆H₂₂N₆O₆S: 547 (MH⁺).

Example 337

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3,3-dimethylbutanamide. MS (EI) m/z C₂₈H₃₁N₅O₅S: 550 (MH⁺).

Example 338

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-methylpentanamide. MS (EI) m/z C₂₈H₃₁N₅O₅S: 550 (MH⁺).

Example 339

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2,2-dimethylbutanamide. MS (EI) m/z C₂₈H₃₁N₅O₅S: 550 (MH⁺).

Example 340

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-4-methylpentanamide. MS (EI) m/z C₂₈H₃₁N₅O₅S: 550 (MH⁺).

Example 341

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)pyrimidine-5-carboxamide. MS (EI) m/z C₂₇H₂₃N₇O₅S: 558 (MH⁺).

Example 342

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-methylfuran-2-carboxamide. MS (EI) m/z C₂₈H₂₅N₅O₆S: 560 (MH⁺).

Example 343

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)thiophene-3-carboxamide. MS (EI) m/z C₂₇H₂₃N₅O₅S₂: 562 (MH^(f)).

Example 344

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-oxocyclopentanecarboxamide. MS (EI) m/z C₂₈H₂₇N₅O₆S: 562 (MH⁺).

Example 345

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-methoxyethoxy)acetamide. MS (EI) m/z C₂₇H₂₉N₅O₇S: 568 (MH⁺).

Example 346

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-4-methylbenzamide. MS (EI) m/z C₃₀H₂₇N₅O₅S: 570 (MH⁺).

Example 347

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(3-methylisoxazol-4-yl)acetamide. MS (EI) m/z C₂₈H₂₆N₆O₆S: 575 (MH⁺).

Example 348

3-cyclopentyl-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)propanamide. MS (EI) m/z C₃₀H₃₃N₅O₅S: 576 (MH⁺).

Example 349

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-o-tolylacetamide. MS (EI) m/z C₃₁H₂₉N₅O₅S: 584 (MH⁺).

Example 350

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-methoxynicotinamide. MS (EI) m/z C₂₉H₂₆N₆O₆S: 587 (MH⁺).

Example 351

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-4-fluoro-3-methylbenzamide. MS (EI) m/z C₃₀H₂₆FN₅O₅S: 588 (MH⁺).

Example 352

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-fluoro-2-methylbenzamide. MS (EI) m/z C₃₀H₂₆FN₅O₅S: 588 (MH⁺).

Example 353

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-fluoro-4-methylbenzamide. MS (EI) m/z C₃₀H₂₆FN₅O₅S: 588 (MH⁺).

Example 354

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-fluoro-5-methylbenzamide. MS (EI) m/z C₃₀H₂₆FN₅O₅S: 588 (MH⁺).

Example 355

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-5-fluoro-2-methylbenzamide. MS (EI) m/z C₃₀H₂₆FN₅O₅S: 588 (MH⁺).

Example 356

6-chloro-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)nicotinamide. MS (EI) m/z C₂₈H₂₃ClN₆O₅S: 591 (MH⁺).

Example 357

2-chloro-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)nicotinamide. MS (EI) m/z C₂₈H₂₃ClN₆O₅S: 591 (MH⁺).

Example 358

2-chloro-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)isonicotinamide. MS (EI) m/z C₂₈H₂₃ClN₆O₅S: 591 (MH⁺).

Example 359

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-4-(dimethylamino)benzamide. MS (EI) m/z C₃₁H₃₀N₆O₅S: 599 (MH⁺).

Example 360

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-(dimethylamino)benzamide. MS (EI) m/z C₃₁H₃₀N₆O₅S: 599 (MH⁺).

Example 361

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)benzo[d][1,3]-dioxole-5-carboxamide. MS (EI) m/z C₃₀H₂₅N₅O₇S: 600 (MH⁺).

Example 362

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(m-tolyloxy)acetamide. MS (EI) m/z C₃₁H₂₉N₅O₆S: 600 (MH⁺).

Example 363

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(4-methoxyphenyl)acetamide. MS (EI) m/z C₃₁H₂₉N₅O₆S: 600 (MH⁺).

Example 364

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(2-methoxyphenyl)acetamide. MS (EI) m/z C₃₁H₂₉N₅O₆S: 600 (MH⁺).

Example 365

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(3-methoxyphenyl)acetamide. MS (EI) m/z C₃₁H₂₉N₅O₆S: 600 (MH⁺).

Example 366

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-methoxy-4-methylbenzamide. MS (EI) m/z C₃₁H₂₉N₅O₆S: 600 (MH⁺).

Example 367

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-fluoro-4-methoxybenzamide. MS (EI) m/z C₃₀H₂₆FN₅O₆S: 604 (MH⁺).

Example 368

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-fluoro-6-methoxybenzamide. MS (EI) m/z C₃₀H₂₆FN₅O₆S: 604 (MH⁺).

Example 369

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-(4-methoxyphenyl)propanamide. MS (EI) m/z C₃₂H₃₁N₅O₆S: 614 (MH⁺).

Example 370

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-(2-methoxyphenyl)propanamide. MS (EI) m/z C₃₂H₃₁N₅O₆S: 614 (MH⁺).

Example 371

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-(3-methoxyphenyl)propanamide. MS (EI) m/z C₃₂H₃₁N₅O₆S: 614 (MH⁺).

Example 372 N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)azetidine-3-carboxamide

Into a 20 mL vial was added 3-amino-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide (0.24 mmol, 1 equiv), prepared using procedures similar to those described in Example 15, DMA (5 mL) and 1-(tert-butoxycarbonyl)azetidine-3-carboxylic acid (0.336 mmol, 1.4 equiv). Hunig's Base (0.792 mmol, 3.3 equiv) and HATU (0.288 mmol, 1.2 equiv) were added to the vial and the reaction mixture was then stirred at room temperature overnight. Completion of the reaction was indicated by LCMS. The solvent was removed by rotary evaporation. The crude mixture was carried forward without further purification. The residue was suspended in 5 mL ethyl acetate and chilled in an ice bath. A solution of 4 N HCl in dioxane (3 mL, 5 equiv) was added with stirring. The reaction mixture was then stirred at room temperature overnight. The solid materials were collected by filtration, washed with ethylacetate then purified further by preparative reverse-phase HPLC (ammonium acetate/ACN). A Waters Fractionlynx preparative reverse-phase HPLC; equipped with a Waters SunFire Prep C18, OCD 5 μM, 30×70 mm column and running a 5-100% gradient with a binary solvent system of 25 mM ammonium acetate in water/acetonitrile; was used to carry out the purification. N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)azetidine-3-carboxamide was obtained (26 mg, 20%). ¹H-NMR (400 MHz, d₆-DMSO): 10.26 (s, 1H), 8.81 (s, 1H), 8.25 (t, 8.14 (s, 1H), 7.74 (d, 1H), 7.69 (d, 1H), 7.41-7.39 (m, 1H), 7.36 (d, 1H), 7.32 (d, 2H), 7.30-7.28 (dd, 1H), 7.14-7.11 (m, 2H), 6.14 (t, 1H), 4.09 (d, 4H), 3.78 (s, 6H); MS (EI) m/z C₂₆H₂₆N₆O₅S: 535.6 (MH⁺).

Example 373 N-(3-(4-fluorophenylamino)quinoxalin-2-yl)benzenesulfonamide

A flask was charged with 2,3-dichloroquinoxaline (3.5 g, 18 mmol), 85 mL of dimethylsulfoxide, benzene sulfonamide (2.8 g, 18 mmol), and cesium carbonate (5.8 g, 18 mmol). The reaction mixture was stirred under an N₂ atmosphere for 15 h at 150° C., after which time, it was transferred to a separatory funnel and 100 mL of water were added. Concentrated HCl was then added in order to acidify the reaction mixture to pH<2. The aqueous layer was subsequently washed three times with 90 mL ethyl acetate. The ethyl acetate layers were then washed two times with 150 mL water, three times with 100 mL brine and then dried over sodium sulfate. The ethyl acetate was removed on a rotary-evaporator. A slurry was formed by adding ethyl acetate and dichloromethane to the dried crude product, filtration yielded N-(3-chloroquinoxalin-2-yl)-benzenesulfonamide which was used without further purification. MS (EI) m/z C₁₄H₁₀ClN₃O₂S: 319.9 (MH⁺).

A CEM microwave reaction vessel was charged with N-(3-chloroquinoxalin-2-yl)benzenesulfonamide (52 mg, 0.16 mmol), prepared using procedures similar to those described in the above step, 4-fluoroaniline (36 mg, 0.32 mmol), and 0.8 mL of dimethylacetamide. The vessel was sealed and the reaction mixture was heated under microwave radiation for 25 m at 120° C. in a CEM Discover microwave instrument. Methanol (1 mL) was added to the reaction mixture and after 20 minutes the product precipitated out of the solution. Filtration yielded N-(3-(4-fluorophenylamino)quinoxalin-2-yl)benzenesulfonamide (39 mg, 62%). ¹H-NMR (400 MHz, d_(o)-DMSO): δ 12.30 (s, 1H), 9.11 (s, 1H), 8.16-8.10 (d, 2H), 8.02-7.90 (m, 3H), 7.68-7.58 (m, 3H), 7.55-7.51 (m, 1H), 7.41-7.32 (m, 2H), 7.25-7.16 (m, 2H); MS (EI) m/z C₂₀H₁₅FN₄O₂S: 395.0 (MH⁺).

Example 374 N-(3-(N-(3-chloroquinoxalin-2-yl)sulfamoyl)phenyl)-2-(dimethylamino)acetamide

Scheme A

A flask was charged with 3-aminobenzene sulfonamide (3.3 g, 19 mmol), and 20 mL of 1:1 acetone:H₂O. The solution was stirred at room temperature until the aminobenzene sulfonamide had dissolved. The flask was then cooled in an ice bath and dimethylamino-acetyl chloride HCl (4.6 g, 29 mmol) was added. To the resulting slurry sodium bicarbonate (4.8 g, 57 mmol) was added over a 15 m period. After 30 min the reaction was removed from the ice bath and allowed to stir at room temperature for 15 h. The reaction mixture was then filtered and washed with methanol and acetonitrile. The filtrate was dried on a rotary evaporator to yield 2-(dimethylamino)-N-(3-sulfamoyl-phenyl)acetamide, which was submitted to the next step without further purification. MS (EI) m/z C₁₀H₁₅N₃O₃S: 258.0 (MH⁺).

Scheme B

A flask was charged with dichloroquinozaline (1.0 g, 5.8 mmol), 10 mL of dimethylacetamide, 2-(dimethylamino)-N-(3-sulfamoylphenyl)acetamide (0.70 g, 2.7 mmol), and cesium carbonate (1.8 g, 5.5 mmol). The reaction mixture was stirred for 3 h at 140° C. and then filtered. The solvent was evaporated from the filtrate on a rotary-evaporator to yield (N-(3-(N-(3-chloroquinoxalin-2-yl)sulfamoyl)phenyl)-2-(dimethylamino)acetamide) which was submitted to the next step without further purification. MS (EI) m/z C₁₈H₁₈ClN₅O₃S: 420.0 (MH⁺).

General Amination Procedure 1a

A CEM microwave reaction vessel was charged with N-(3-(N-(3-chloroquinoxalin-2-yl)sulfamoyl)phenyl)-2-(dimethylamino)acetamide (30 mg, 0.071 mmol), prepared using procedures similar to those described in Example 374, the desired aniline (16 mg, 0.14 mmol, 2 eq), and 0.5 mL of dimethylacetamide. The vessel was sealed and the reaction mixture was heated under microwave radiation for 70 min at 140° C. in a CEM Discover microwave instrument. The solvent was then removed by rotary-evaporation. Purification of the final product was accomplished by preparatory reverse-phase HPLC with the eluents 25 mM aqueous NH₄OAc/ACN to the desired product.

The following compounds were prepared according to the above General Amination Procedure 1a.

Example 375 2-(dimethylamino)-N-(3-(N-(3-(3-fluorophenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. ¹H-NMR (400 MHz, CDCl₃): 9.40 ppm (s, 1H), 8.43 ppm (s, 1H), 8.22 ppm (s, 1H), 8.07-8.02 ppm (d, 1H), 7.97-7.93 ppm (d, 1H), 7.76-7.71 (m, 2H), 7.53-7.48 ppm (t, 1H), 7.45-7.36 ppm (m, 4H), 7.35-7.28 ppm (m, 2H), 6.84-6.77 ppm (t, 1H), 3.10 ppm (s, 2H), 2.38 ppm (s, 6H); MS (EI) m/z C₂₄H₂₃FN₆O₃S: 495 (MH⁺). Example 376

2-(dimethylamino)-N-(3-(N-(3-(4-fluorophenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₂₄H₂₃FN₆O₃S: 495 (MH⁺).

Example 377

N-(3-(N-(3-(4-chloro-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(dimethylamino)acetamide. MS (EI) m/z C₂₄H₂₃ClN₆O₃S: 511 (MH⁺).

General Amination Procedure 1b

A CEM microwave reaction vessel was charged with N-(3-(N-(3-chloroquinoxalin-2-yl)sulfamoyl)phenyl)-2-(dimethylamino)acetamide (62 mg, 0.147 mmol), prepared using procedures similar to those in Example 374, the desired aniline (0.567 mmol, 4 eq), and 1.0 mL of toluene. The vessel was sealed and the reaction mixture was heated under microwave radiation for 60 min at 180° C. in a CEM Discover microwave instrument. The solvent was removed on a rotary-evaporator. Purification of the final product was done by preparatory HPLC with NH₄OAc/ACN as eluent to yield the desired product.

The following compounds were prepared according to the above General Amination Procedure 1b.

Example 378

N-(3-(N-(3-(3-chloro-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-2-(dimethylamino)acetamide. MS (EI) m/z C₂₄H₂₃ClN₆O₃S: 511 (MH⁺).

Example 379

2-(dimethylamino)-N-(3-(N-(3-(4-fluoro-3-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. 2-(dimethylamino)-N-(3-(N-(3-(4-fluoro-3-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl). ¹H-NMR (400 MHz, CDCl₃): δ 9.47 (s, 1H), 8.36 (s, 1H), 8.29 (s, 1H), 7.91-7.87 (d, 1H), 7.80-7.73 (m, 2H), 7.66-7.63 (d, 1H), 7.53-7.47 (t, 1H), 7.43-7.30 (m, 4H), 7.10-7.04 (t, 1H), 6.55-5.95 (br s, 1H), 3.96 (s, 3H), 3.12 (s, 2H), 2.39 (s, 6H), 2.08 (s, 3H(AcOH); MS (EI) m/z C₂₅H₂₅FN₆O₄S: 525 (MH⁺).

Example 380 N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-4-isopropoxybenzenesulfonamide

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-4-isopropoxy-benzenesulfonamide. A solution of 2,3-dichloroquinoxaline (2.0 mL, 0.38 M) was combined with K₂CO₃ (105 mg, 0.76 mmol) in a glass vial. A solution of 4-isopropoxybenzene sulfonamide (1.75 mL, 0.43 M) was added and the solution was stirred overnight at 125° C. After cooling, acetic acid (45 mL, 0.79 mmol) and 3,5-dimethoxyaniline (230 mg, 1.5 mmol) were added. The reaction mixture was stirred again at 125° C. overnight. Upon cooling, the reaction mixture was diluted with 8 mL of methanol and then 8 mL of water. The precipitate was collected by filtration and recrystallized from N,N-dimethylacetamide/water to give N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-4-isopropoxy-benzenesulfonamide (45 mg, 12%). ¹H-NMR (400 MHz, d₆-DMSO): 12.16 (bs, 1H), 8.93 (s, 1H), 8.03 (d, 2H), 7.92 (bs, 1H), 7.56 (d, 1H), 7.36 (m, 4H), 7.07 (d, 2H), 6.24 (s, 1H), 4.72 (m, 1H), 3.76 (s, 6H), 1.27 (d, 6H); MS (EI) m/z C₂₅H₂₆N₄O₅S: 495 (MH⁺).

Examples 381-411 were synthesized proceeding as above in Example 423. In the cases where the product did not precipitate, the mixture was purified by reverse phase HPLC.

Example 381

3-chloro-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-4-methylbenzenesulfonamide. ¹H-NMR (400 MHz, d₆-DMSO): 12.31 (bs, 1H), 8.96 (s, 1H), 8.18 (s, 1H), 7.98 (d, 1H), 7.92 (bs, 1H), 7.58 (d, 2H), 7.43-7.33 (m, 4H), 6.24 (t, 1H), 3.76 (s, 6H), 2.39 (s, 3H); MS (EI) m/z C₂₃H₂₁ClN₄O₄S: 485 (MH⁺).

Example 382

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)naphthalene-1-sulfonamide. MS (EI) m/z C₂₆H₂₂N₄O₄S: 487 (MH⁺).

Example 383

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-4-fluorobenzenesulfonamide. MS (EI) m/z C₂₂H₁₉FN₄O₄S: 455 (MH⁺).

Example 384

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-3-fluorobenzenesulfonamide. MS (EI) m/z C₂₂H₁₉FN₄O₄S: 455 (MH⁺).

Example 385

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-3-(trifluoromethyl)benzenesulfonamide. MS (EI) m/z C₂₃H₁₉F₃N₄O₄S: 505 (MH⁺).

Example 386

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-4-(trifluoromethyl)benzenesulfonamide. MS (EI) m/z C₂₃H₁₉F₃N₄O₄S: 505 (MH⁺).

Example 387

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-4-(trifluoromethoxy)benzenesulfonamide. MS (EI) m/z C₂₃H₁₉F₃N₄O₅S: 521 (MH⁺).

Example 388

N-(4-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)acetamide. MS (EI) m/z C₂₄H₂₃N₅O₅S: 494 (MH⁺).

Example 389

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-4-fluoro-2-methylbenzenesulfonamide. MS (EI) m/z C₂₃H₂₁FN₄O₄S: 469 (MH⁺).

Example 390

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-2-methylbenzenesulfonamide. MS (EI) m/z C₂₃H₂₂N₄O₄S: 451 (MH⁺).

Example 391

2-chloro-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z C₂₂H₁₉ClN₄O₄S: 471 (MH⁺).

Example 392

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-3,5-difluorobenzenesulfonamide. MS (EI) m/z C₂₂H₁₈F₂N₄O₄S: 473 (MH⁺).

Example 393

3,5-dichloro-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z C₂₂H₁₈Cl₂N₄O₄S: 505 (MH⁺).

Example 394

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-3-fluoro-4-methylbenzenesulfonamide. MS (EI) m/z C₂₃H₂₁FN₄O₄S: 469 (MH⁺).

Example 395

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-2-(trifluoromethyl)benzenesulfonamide. MS (EI) m/z C₂₃H₁₉F₃N₄O₄S: 505 (MH⁺).

Example 396

4-cyano-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z C₂₃H₁₉N₅O₄S: 462 (MH⁺).

Example 397

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-1-phenylmethanesulfonamide. MS (EI) m/z C₂₃H₂₂N₄O₄S: 451 (MH⁺).

Example 398

4,5-dichloro-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)thiophene-2-sulfonamide. MS (EI) m/z C₂₀H₁₆Cl₂N₄O₄S₂: 511 (MH⁺).

Example 399

1-(3-chlorophenyl)-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)methanesulfonamide. MS (EI) m/z C₂₃H₂₁ClN₄O₄S: 485 (MH⁺).

Example 400

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-2,5-dimethylthiophene-3-sulfonamide. MS (EI) m/z C₂₂H₂₂N₄O₄S₂: 471 (MH⁺).

Example 401

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-3,5-bis(trifluoromethyl)benzenesulfonamide. MS (EI) m/z C₂₄H₁₈F₆N₄O₄S: 573 (MH⁺).

Example 402

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-4-fluoro-3-(trifluoromethyl)benzenesulfonamide. MS (EI) m/z C₂₃H₁₈F₄N₄O₄S: 523 (MH⁺).

Example 403

5-chloro-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-1,3-dimethyl-1H-pyrazole-4-sulfonamide. MS (EI) m/z C₂₁H₂₁ClN₆O₄S: 489 (MH⁺).

Example 404 5-chloro-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-2-methoxybenzenesulfonamide. MS (EI) m/z C₂₃H₂₁ClN₄O₅S: 501 (MH⁺). Example 405 5-bromo-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-2-methoxybenzenesulfonamide. MS (EI) m/z C₂₃H₂₁BrN₄O₅S: 545 (MH⁺). Example 406 2,5-dichloro-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)thiophene-3-sulfonamide. MS (EI) m/z C₂₀H₁₆Cl₂N₄O₄S₂: 511 (MH⁺). Example 407

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-3,5-dimethylisoxazole-4-sulfonamide. MS (EI) m/z C₂₁H₂₁N₅O₅S: 456 (MH⁺).

Example 408

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-2,5-dimethoxybenzenesulfonamide. MS (EI) m/z C₂₄H₂₄N₄O₆S: 497 (MH⁺).

Example 409

3-chloro-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-4-fluorobenzenesulfonamide. MS (EI) m/z C₂₂H₁₈ClFN₄O₄S: 489 (MH⁺).

Example 410

4-(difluoromethoxy)-N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide MS (EI) m/z C₂₃H₂₀F₂N₄O₅S: 503 (MIT).

Example 411

N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-3-(methylsulfonyl)benzenesulfonamide. MS (EI) m/z C₂₃H₂₂N₄O₆S₂: 515 (MH⁺).

General Acylation Procedure 2

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)-sulfamoyl)phenyl)azetidine-3-carboxamide (125 mg, 0.23 mmol), prepared using procedures similar to those described in Example 372, was dissolved into 5 mL DCE in a 10 mL round-bottom flask. DIEA (1.17 mmol, 5.0 equiv.) was then added with stirring followed by acid chloride (0.47 mmol, 2.0 equiv.). The reaction was then stirred at room temperature for 1 hour or until complete as indicated by LCMS. The solvent was subsequently removed under reduced pressure on a rotary evaporator. The crude material was then redissolved in methanol. Purification of the final product was accomplished by preparatory reverse-phase HPLC with the eluents 25 mM aqueous NH₄OAc/CAN. A Waters Fractionlynx preparative reverse-phase HPLC; equipped with a Waters SunFire Prep C18, OCD 5 μM, 30×70 mm column and running a 5-100% gradient with a binary solvent system of 25 mM ammonium acetate in water/acetonitrile; was used to carry out the purification.

The following compounds were prepared according to General Acylation Procedure 2.

Example 412

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-1-propionylazetidine-3-carboxamide. ¹H-NMR (400 MHz, d₆-DMSO): 12.40 (s, 1H), 10.45 (s, 1H), 8.88 (s, 1H), 8.40 (s, 1H), 7.93 (s, 1H), 7.82 (d, 1H), 7.77 (d, 1H), 7.60-7.45 (m, 2H), 7.41-7.30 (m, 4H), 6.24 (s, 1H), 4.26 (t, 1H), 4.22-4.17 (m, 1H), 3.99 (t, 1H), 3.95-3.89 (m, 1H), 3.76 (s, 6H), 3.59-3.45 (m, 1H), 2.05 (dd, 2H), 0.95 (t, 3H); MS (EI) m/z C₂₉H₃₀N₆O₆S: 591 (MH⁺).

Example 413

1-acetyl-N-(3-{[(3-{[3,5-bis(methoxy)-phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)azetidine-3-carboxamide. MS (EI) m/z C₂₈H₂₈N₆O₆S: 577 (MH⁺).

Example 414

1-(cyclopropanecarbonyl)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)azetidine-3-carboxamide. MS (EI) m/z C₃₀H₃₀N₆O₆S: 603 (MH⁺).

General Reductive Amination Procedure 1

To a solution of N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)azetidine-3-carboxamide (110 mg, 0.19 mmol), prepared using procedures similar to those described in Example 372, in 3 mL of DCE and 200 μL of DMF, aldehyde (0.77 mmol, 4.0 eq.)was added slowly followed by tetramethylammonium triacetoxyborohydride (1.16 mmol, 6.0 eq). The reaction was stirred at room temperature overnight. LC/MS indicated the reaction was completed. The solvent was subsequently removed under reduced pressure on a rotary evaporator. The crude material was then redissolved in methanol. Purification of the final product was accomplished by preparatory reverse-phase HPLC with the eluents 25 mM aqueous NH₄OAc/CAN. A Waters Fractionlynx preparative reverse-phase HPLC; equipped with a Waters SunFire Prep C18, OCD 5 μM, 30×70 mm column and running a 5-100% gradient with a binary solvent system of 25 mM ammonium acetate in water/acetonitrile; was used to carry out the purification.

The following title compounds were prepared according to General Reductive Amination Procedure 1.

Example 415

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-1-ethylazetidine-3-carboxamide. ¹H-NMR (400 MHz, d₆-DMSO): 10.29 (s, 1H), 8.82 (s, 1H), 8.25 (t, 1H), 7.75-7.68 (m, 2H), 7.43-7.38 (m, 1H), 7.375-7.340 (m, 1H), 7.338-7.310 (d, 2H), 7.305-7.262 (m, 1H), 7.15-7.08 (m, 2H), 6.56 (s, 1H), 6.15 (t, 1H), 4.15-4.08 (m, 2H), 4.06-3.95 (m, 2H), 3.78 (s, 6H), 3.65-3.56 (m, 1H), 3.12-3.04 (m, 2H), 1.03 (t, 3H); MS (EI) m/z C₂₈H₃₀N₆O₅S: 563 (MH⁺).

Example 416

1-(cyclopropylmethyl)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)azetidine-3-carboxamide. MS (EI) m/z C₃₀H₃₂N₆O₅S: 589 (MH⁺).

Example 417

1-benzyl-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)azetidine-3-carboxamide. MS (EI) m/z C₃₃H₃₂N₆O₅S: 625 (MH⁺).

Example 418

N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-1-(furan-2-ylmethyl)azetidine-3-carboxamide. MS (EI) m/z C₃₁H₃₀N₆O₆S: 615 (MH⁺).

Example 419

1-((1H-imidazol-5-yl)methyl)-N-(3-(N-(3-(3,5-dimethoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)azetidine-3-carboxamide. MS (EI) m/z C₃₀H₃₀N₈O₅S: 615 (MH⁺).

General Amide Formation Procedure 1a

Into a small 1 dram vial was added 3-(N-(3-(2-chloro-5-methoxy-phenylamino)-quinoxalin-2-yl)sulfamoyl)benzoic acid (61 mg, 0.13 mmol, 1.1 equiv), prepared using procedures described for Example 100. The acid was dissolved in DMA (1 mL) and DIEA (42 μL, 0.24 mmol, 2 equiv) was added then added to the solution. The amine reagent (1 mL of 0.12 M solution in DMA) was added to solution with stirring followed by HATU (64 mg, 0.17 mmol, 1.4 equiv). The reaction was stirred overnight at room temperature. Upon completion as indicated by LCMS analysis, 2 mL of methanol was added to the solution. Preparative reverse-phase HPLC was used to isolate the desired product. A Waters Fractionlynx preparative reverse-phase HPLC—equipped with a Waters SunFire Prep C18, OCD 5 μM, 30×70 mm column and running a 5-100% gradient with a binary solvent system of 25 mM ammonium acetate in water/acetonitrile—was used to carry out the purification.

The following compounds were prepared according to General Amide Formation Procedure 1.

Example 420

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(3-(dimethylamino)propyl)benzamide. 3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)-N-(3-(dimethylamino)propyl)benzamide: NMR (400 MHz, d₆-DMSO): 9.44 (s, 1H), 8.94 (s, 1H), 8.79 (t, 1H), 8.54 (s, 1H), 8.24 (d, 1H), 7.87 (d, 1H), 7.48 (m, 3H), 7.33 (d, 1H), 7.18 (m, 2H), 6.60 (dd, 1H), 3.82 (1H), 3.04 (m, 3H), 2.51 (m, 5H), 1.91 (s, 1H), 1.86 (m, 3H); MS (EI) m/z for C₂₇H₂₉ClN₆O₄S: 569 (MH⁺).

Example 421

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(1-methylazetidin-3-yl)benzamide. 3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)-N-(1-methylazetidin-3-yl)benzamide: ¹H NMR (400 MHz, d₆-DMSO): 9.43 (s, 1H), 9.23 (d, 1H), 8.94 (d, 1H), 8.58 (s, 1H), 8.29 (d, 1H), 7.89 (d, 1H), 7.56 (t, 1H), 7.47 (d, 1H), 7.44 (d, 1H), 7.33 (d, 1H), 7.18 (m, 2H), 6.60 (dd, 1H), 4.81 (m, 1H), 4.33 (m, 2H), 4.19 (m, 2H), 3.82 (s, 1H), 2.51 (s, 3H); MS (EI) m/z for C₂₆H₂₅ClN₆O₄S: 553 (MH⁺).

Example 422

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(pyridin-4-ylmethyl)benzamide. MS (EI) m/z C₂₈H₂₃ClN₆O₄S: 575 (MH⁺).

Example 423

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(3-(dimethylamino)propyl)benzamide. MS (EI) m/z C₂₈H₂₆ClN₇O₄S: 592 (MH⁺).

Example 424

N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)-3-(2,2-dimethylhydrazinecarbonyl)benzenesulfonamide. MS (EI) m/z C₂₄H₂₃ClN₆O₄S: 527 (MH⁺).

Example 425

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-methoxyethyl)benzamide. MS (EI) m/z C₂₅H₂₄ClN₅O₅S: 542 (MH⁺).

Example 426

N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)-3-(4-methylpiperazine-1-carbonyl)benzenesulfonamide. MS (EI) m/z C₂₇H₂₇ClN₆O₄S: 567 (MH⁺).

Example 427

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-(pyrrolidin-1-yl)ethyl)benzamide. MS (EI) m/z C₂₈H₂₉ClN₆O₄S: 581 (MH⁺).

Example 428

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-(pyridin-4-yl)ethyl)benzamide. MS (EI) m/z C₂₉H₂₅ClN₆O₄S: 589 (MH⁺).

Example 429

N-(2-(1H-imidazol-4-yl)ethyl)-3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)benzamide. MS (EI) m/z C₂₇H₂₄ClN₇O₄S: 578 (MH⁺).

Example 430

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(piperidin-1-yl)benzamide. MS (EI) m/z C₂₇H₂₇ClN₆O₄S: 567 (MH⁺).

Example 431

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-hydroxyethyl)benzamide. MS (EI) m/z C₂₄H₂₂ClN₅O₅S: 528 (MH⁺).

Example 432

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(3-ethoxypropyl)benzamide. MS (EI) m/z C₂₇H₂₈ClN₅O₅S: 570 (MH⁺).

Example 433

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(3-(pyrrolidin-1-yl)propyl)benzamide. MS (EI) m/z C₂₉H₃₁ClN₆O₄S: 595 (MH⁺).

Example 434

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(3-(diethylamino)propyl)benzamide. MS (EI) m/z C₂₉H₃₃ClN₆O₄S: 597 (MH⁺).

Example 435

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(3-(2-oxopyrrolidin-1-yl)propyl)benzamide. MS (EI) m/z C₂₉H₂₉ClN₆O₅S: 609 (MH⁺).

Example 436

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(pyridin-2-ylmethyl)benzamide. MS (EI) m/z C₂₈H₂₃ClN₆O₄S: 575 (MH⁺).

Example 437

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-cyanoethyl)-N-methylbenzamide. MS (EI) m/z C₂₆H₂₃ClN₆O₄S: 551 (MH⁺).

Example 438

3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-cyanoethyl)-N-ethylbenzamide. MS (EI) m/z C₂₇H₂₅ClN₆O₄S: 565 (MH⁺).

Example 439

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-(ethylthio)ethyl)benzamide. MS (EI) m/z C₂₆H₂₆ClN₅O₄S₂: 572 (MH⁺).

Example 440

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(3-propoxypropyl)benzamide. MS (EI) m/z C₂₈H₃₀ClN₅O₅S: 584 (MH⁺).

Example 441

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(5-(diethylamino)pentan-2-yl)benzamide. MS (EI) m/z C₃₁H₃₇ClN₆O₄S: 625 (MH⁺).

Example 442

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(3-methoxypropyl)benzamide. MS (EI) m/z C₂₆H₂₆ClN₅O₅S: 556 (MH⁺).

Example 443

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(3-morpholinopropyl)benzamide MS (EI) m/z C₂₉H₃₁ClN₆O₅S: 611 (MH⁺).

Example 444

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(pyridin-3-ylmethyl)benzamide MS (EI) m/z C₂₈H₂₃ClN₆O₄S: 575 (MH⁺).

Example 445

3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-cyanoethyl)benzamide. MS (EI) m/z C₂₅H₂₁ClN₆O₄S: 537 (MH⁺).

Example 446

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(1-methoxypropan-2-yl)benzamide. MS (EI) m/z C₂₆H₂₆ClN₅O₅S: 556 (MH⁺).

Example 447

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-(methylthio)ethyl)benzamide. MS (EI) m/z C₂₅H₂₄ClN₅O₄S₂: 558 (MH⁺).

Example 448

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(3-(dimethylamino)propyl)-N-methylbenzamide. MS (EI) m/z C₂₈H₃₁ClN₆O₄S: 583 (MH⁺).

Example 449

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(3-isopropoxypropyl)benzamide. MS (EI) m/z C₂₈H₃₀ClN₅O₅S: 584 (MH⁺).

Example 450

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-(dimethylamino)ethyl)-N-ethylbenzamide. MS (EI) m/z C₂₈H₃₁ClN₆O₄S: 583 (MH⁺).

Example 451

N-(3-butoxypropyl)-3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)benzamide. MS (EI) m/z C₂₉H₃₂ClN₅O₅S: 598 (MH⁺).

Example 452

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-(diethylamino)ethyl)benzamide. MS (EI) m/z C₂₈H₃₁ClN₆O₄S: 583 (MH⁺).

Example 453

methyl 3-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)benzamido)propanoate. MS (EI) m/z C₂₆H₂₄ClN₅O₆S: 570 (MH⁺).

Example 454

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-methyl-N-propylbenzamide. MS (EI) m/z C₂₆H₂₆ClN₅O₄S: 540 (MH⁺).

Example 455

ethyl 3-(3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)benzamido)propanoate. MS (EI) m/z C₂₇H₂₆ClN₅O₆S: 584 (MH⁺).

Example 456

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-(piperidin-1-yl)ethyl)benzamide. MS (EI) m/z C₂₉H₃₁ClN₆O₄S: 595 (MH⁺).

Example 457

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-((1-ethylpyrrolidin-2-yl)methyl)benzamide. MS (EI) m/z C₂₉H₃₁ClN₆O₄S: 595 (MH⁺).

Example 458

N-(2-(bis(2-hydroxyethyl)amino)ethyl)-3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)benzamide. MS (EI) m/z C₂₈H₃ClN₆O₆S: 615 (MH⁺).

Example 459

N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)-3-(3-(diethylamino)pyrrolidine-1-carbonyl)benzenesulfonamide. MS (EI) m/z C₃₀H₃₃ClN₆O₄S: 609 (MH⁺).

Example 460

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-methyl-N-(1-methylpyrrolidin-3-yl)benzamide. MS (EI) m/z C₂₈H₂₉ClN₆O₄S: 581 (MH⁺).

Example 461

N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)-3-(3-(dimethylamino)pyrrolidine-1-carbonyl)benzenesulfonamide. MS (EI) m/z C₂₈H₂₉ClN₆O₄S: 581 (MH⁺).

Example 462

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(2-methyl-1-morpholinopropan-2-yl)benzamide. MS (EI) m/z C₃₀H₃₃ClN₆O₅S: 625 (MH⁺).

Example 463

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(1H-pyrrol-1-yl)benzamide. MS (EI) m/z C₂₆H₂₁ClN₆O₄S: 549 (MH⁺).

Example 464

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(3-oxopyrazolidin-4-yl)benzamide. MS (EI) m/z C₂₅H₂₂ClN₇O₅S: 568 (MH⁺).

Example 465

N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)-3-(2-((dimethylamino)methyl)piperidine-1-carbonyl)benzenesulfonamide. MS (EI) m/z C₃₀H₃₃ClN₆O₄S: 609 (MH⁺).

Example 466

N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)-3-(2-(piperidin-1-ylmethyl)piperidine-1-carbonyl)benzenesulfonamide. MS (EI) m/z C₃₃H₃₇ClN₆O₄S: 649 (MH⁺).

Example 467

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(1-ethylpiperidin-3-yl)benzamide MS (EI) m/z C₂₉H₃₁ClN₆O₄S: 595 (MH⁺).

General Amide Formation Procedure 1b

The procedure outlined in General Amide Formation Procedure 1a was used to incorporate a number of amines that contained a second amine group protected as the tert-butylcarbamate (i.e. where R′, within NHR′R″, contained a Boc-protected amine group). The deprotection was carried out after HPLC purification of the Boc-protected precursor.

Into a small 1 dram vial was added 3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)benzoic acid (61 mg, 0.13 mmol, 1.1 equiv). The acid was dissolved in 1 mL of DMA and DIEA (42 μL, 0.24 mmol, 2 equiv) was added then added to the solution. The mono-Boc-protected diamine reagent (1 mL of 0.12 M solution in DMA, 1 equiv) was added to solution with stirring followed by HATU (64 mg, 0.17 mmol, 1.4 equiv). The reaction was stirred overnight at room temperature. Upon completion as indicated by LCMS analysis, 2 mL of methanol was added to the solution. Preparative reverse-phase HPLC was used to isolate the desired product directly from this crude reaction solution. A Waters Fractionlynx preparative reverse-phase HPLC; equipped with a Waters SunFire Prep C18, OCD 5 μM, 30×70 mm column and running a 5-100% gradient with a binary solvent system of 25 mM ammonium acetate in water/acetonitrile; was used to carry out the purification. The product fractions were combined and concentrated to dryness under reduced pressure by rotary evaporation. A solution of 4 N HCl in dioxane (2 mL) was added. The solution was then stirred at room temperature until no starting material was detected. The deprotected product precipitated out of solution as an HCL salt and was collected by filtration, washed with ether and dried under vacuum.

The following compounds were prepared according to the above General Amide Formation Procedure 1b.

Example 468

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(piperidin-3-yl)benzamide. 3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)-N-(piperidin-3-yl)benzamide: ¹H NMR (400 MHz, d₆-DMSO): 12.82 (s, 1H), 9.12 (s, 1H), 9.04 (s, 1H), 8.85 (d, 1H), 8.65 (s, 1H), 8.55 (s, 1H), 8.18 (m, 1H), 7.98 (s, 1H), 7.69 (m, 2H), 7.43 (m, 2H), 6.69 (dd, 1H), 4.21 (s, 1H), 3.83 (s, 3H), 3.69 (m, 1H), 3.48 (m, 1H), 3.18 (s, 1H), 2.84 (q, 2H), 1.91 (s, 2H); MS (EI) m/z for C₂₇H₂₇ClN₆O₄S: 567 (MH⁺).

Example 469

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(piperidin-2-ylmethyl)benzamide. 3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)-N-(piperidin-2-ylmethyl)benzamide: NMR (400 MHz, d₆-DMSO): 12.78 (s, 1H), 9.16 (s, 1H), 9.09 (s, 1H), 8.79 (s, 1H), 8.59 (d, 2H), 8.22 (t, 2H), 7.99 (s, 1H), 7.74 (t, 1H), 7.66 (s, 1H), 7.42 (m, 2H), 6.69 (dd, 1H), 3.82 (s, 3H), 3.69 (dd, 1H), 3.57 (m, 1H), 3.50 (m, 3H), 3.22 (s, 2H), 2.82 (d, 1H), 1.68 (m, 5H); MS (EI) m/z for C₂₈H₂₉ClN₆O₄S: 581 (MH⁺).

Example 470

3-(3-aminopyrrolidine-1-carbonyl)-N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z C₂₆H₂₅ClN₆O₄S: 553 (MH⁺).

Example 471

3-(3-aminoazetidine-1-carbonyl)-N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z C₂₅H₂₃ClN₆O₄S: 539 (MH⁺).

Example 472

3-(3-aminopiperidine-1-carbonyl)-N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z C₂₇H₂₇ClN₆O₄S: 567 (MH⁺).

Example 473

3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)-N-(pyrrolidin-3-yl)benzamide. MS (EI) m/z C₂₆H₂₅ClN₆O₄S: 553 (MH⁺).

Example 474

N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)-3-(3-(methylamino)pyrrolidine-1-carbonyl)benzenesulfonamide. MS (EI) m/z C₂₇H₂₇ClN₆O₄S: 567 (MH⁺).

Example 475

N-(2-aminoethyl)-3-(N-(3-(2-chloro-5-methoxy-phenylamino)quinoxalin-2-yl)sulfamoyl)benzamide. MS (EI) m/z C₂₄H₂₃ClN₆O₄S: 527 (MH⁺).

Example 476

3-(4-amino-3-oxopyrazolidine-1-carbonyl)-N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)benzenesulfonamide. MS (EI) m/z C₂₅H₂₂ClN₇O₅S: 568 (MH⁺).

Example 477 3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)-N-((1-methylpiperidin-2-yl)methyl)benzamide

3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)-N-(piperidin-2-ylmethyl)benzamide (299 mg, 0.51 mmol, 1 equiv), prepared using procedures similar to those described for Example 514, was dissolved in 2.3 mL of DMA. Formic acid (388 μL, 10.28 mmol, 20 equiv) was added to solution with stirring followed by the addition of formaldehyde (508 μL of 37% aq. solution). The reaction was then stirred at room temperature overnight. Analysis of an aliquot of the reaction mixture by LCMS indicated the complete consumption of starting material. The reaction was diluted with methanol (2 mL). Preparative reverse-phase HPLC was used to isolate the desired product directly from the crude reaction mixture. A Waters Fractionlynx preparative reverse-phase HPLC; equipped with a Waters SunFire Prep C18, OCD 5 μM, 30×70 mm column and running a 5-100% gradient with a binary solvent system of 25 mM ammonium acetate in water/acetonitrile; was used to carry out the purification. ¹H NMR (400 MHz, d₆-DMSO): 9.44 (s, 1H), 8.94 (s, 1H), 8.79 (t, 1H), 8.57 (s, 1H), 8.27 (d, 1H), 7.90 (d, 1H) 7.54 (t, 1H), 7.46 (d, 1H), 7.39 (d, 1H), 7.33 (d, 1H), 7.18 (m, 2H), 6.60 (dd, 1H), 3.82 (s, 3H), 3.59 (m, 2H), 3.00 (s, 1H), 2.90 (s, 3H), 1.62 (m, 7H); MS (EI) m/z for C₂₉H₃₁ClN₆O₄S: 595 (MH⁺).

Example 478 3-(N-(3-(2-chloro-5-methoxyphenylamino)quinoxalin-2-yl)sulfamoyl)-N-(1-methylpiperidin-3-yl)benzamide

The title compound was prepared using similar procedures to those used in Example 522. ¹H NMR (400 MHz, d₆-DMSO): 9.43 (s, 1H), 8.93 (s, 1H), 8.59 (s, 1H), 8.24 (d, 1H), 7.87 (d, 1H), 7.47 (m, 2H), 7.40 (d, 1H), 7.33 (d, 1H), 7.19 (m, 2H), 6.60 (dd, 1H), 4.21 (s, 1H), 3.82 (s, 1H), 2.76 (s, 1H), 2.50 (m, 7H), 1.91 (m, 2H), 1.63 (m, 2H); MS (EI) m/z for C₂₈H₂₉ClN₆O₄S: 581 (MH⁺).

BIOLOGICAL EXAMPLES Biological Example 1 PI3Kalpha Luciferase-Coupled Chemiluminescence Assay Protocol

PI3Kα activity is measured as the percent of ATP consumed following the kinase reaction using luciferase-luciferin-coupled chemiluminescence. Reactions were conducted in 384-well white, medium binding microtiter plates (Greiner). Kinase reactions were initiated by combining test compounds, ATP, substrate (PIP2), and kinase in a 20 μL volume in a buffer solution. The standard PI3Kalpha assay buffer is composed 50 mM Tris, pH 7.5, 1 mM EGTA, 10 mM MgCl₂, 1 mM DTT and 0.03% CHAPS. The standard assay concentrations for enzyme, ATP, and substrate are 0.5-1.1 nM, 1 μM, and 7.5 μM, respectively. The reaction mixture was incubated at ambient temperature for approximately 2 h. Following the kinase reaction, a 100 μL aliquot of luciferase-luciferin mix (Promega Kinase-Glo) was added and the chemiluminescence signal measured using a Victor2 plate reader (Perkin Elmer). Total ATP consumption was limited to 40-60% and IC₅₀ values of control compounds correlate well with literature references.

Certain compounds of the invention demonstrated the ability to bind to PI3K when tested in this assay. The following embodiments are directed to the compounds themselves as well as their use in a method of treating. For example, in one embodiment of the invention, the PI3K inhibitor is selected from the compounds in Table 1 having a PI3K-binding affinity of about 8 μM or less. In another embodiment, the PI3K inhibitor is selected from the compounds in Table 1 having a PI3K-binding affinity of about 4 μM or less. In another embodiment, the PI3K inhibitor is selected from the compounds in Table 1 having a PI3K-binding affinity of about 3 μM or less. In another embodiment, the PI3K inhibitor is selected from the compounds in Table 1 having a PI3K-binding affinity of about 2 μM or less. In another embodiment, the PI3K inhibitor is selected from the compounds in Table 1 having a PI3K-binding affinity of about 1.5 μM or less. In another embodiment, the PI3K inhibitor is selected from the compounds in Table 1 having a PI3K-binding affinity of about 1.5 μM or less. In another embodiment, the PI3K inhibitor is selected from the compounds in Table 1 having a PI3K-binding affinity of about 0.750 μM or less. In another embodiment, the PI3K inhibitor is selected from the compounds in Table 1 having a PI3K-binding affinity of about 0.5 μM or less. In another embodiment, the PI3K inhibitor is selected from the compounds in Table 1 having a PI3K-binding affinity of about 0.3 μM or less. In another embodiment, the PI3K inhibitor is selected from the compounds in Table 1 having a PI3K-binding affinity of about 0.2 μM or less. In another embodiment, the PI3K inhibitor is selected from the compounds in Table 1 having a PI3K-binding affinity of about 0.1 μM or less. In another embodiment, the PI3K inhibitor is selected from the compounds in Table 1 having a PI3K-binding affinity of about 0.075 μM or less. In another embodiment, the PI3K inhibitor is selected from the compounds in Table 1 having a PI3K-binding affinity of about 0.050 μM or less.

Biological Example 2 Phospho AKT Assay

PC-3 cells were seeded on 6-well plates at 150,000 cells/well. Cells were cultured for 3 days, then treated with compounds in serum-free medium for 3 hr. EGF (100 ng/ml) was added for the last 10 min. Cells were lysed in TENN buffer. Phospho T308 Akt and total Akt were quantfied by ELISA performed according to the Biosource assay protocol. The readings of phospho Akt were normalized to total Akt readings.

Biological Example 3 Phospho S6 Assay

PC-3 cells were seeded on 96-well plates at 8,000 cells/well. For each experiment, cells were seeded and treated in duplicated plates: one plate for phospho S6 CellELISA, and one plate for total S6 CellELISA. Cells were cultured on the plates for 3 days, then treated with compounds in serum-free medium for 3 hr in triplicate. Cells were fixed with 4% formaldehyde, quenched with 0.6% H2O2, blocked with 5% BSA, incubated with either phospho S6 antibody or total S6 antibody overnight, incubated with goat-anti-rabbit-IgG-HRP for 1 hr, and developed in chemiluminescent substrate.

Biological Example 4 PIP₃ Assay

MCF-7 cells grown in 10-cm dishes were starved for 3 hours in DMEM, and then treated with compounds for 20 minutes. In the last 2 minutes of the incubation with the compounds, EGF (100 ng/ml) was added to stimulate the production of PIP3. The medium was aspirated and the cells were scraped with 10% trichloroacetic acid. The lipids were extracted from the pellet after the cell lysates were centrifuged. PIP3 in the cellular lipid extraction was quantified with the AlphaScreen [Registered TM of PerkinElmer] assay in which Grp1-PH is used as the PIP3 specific probe. The amount of cellular PIP3 was calculated from the standard curve of diC₈ PI (3,4,5) P3.

Biological Example 5-10 In Vivo Models

Compound A is a Compound of Formula I. Compound B is N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta-[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine.

Female and male athymic nude mice (NCr) 5-8 weeks of age and weighing approximately 20-25 g were used in the following model. Prior to initiation of a study, the animals were allowed to acclimate for a minimum of 48 h. During these studies, animals were provided food and water ad libitum and housed in a room conditioned at 70-75° F. and 60% relative humidity. A12 h light and 12 h dark cycle was maintained with automatic timers. All animals were examined daily for compound-induced or tumor-related deaths.

PC-3 human prostate adenocarcinoma cells were cultured in vitro in DMEM (Mediatech) supplemented with 20% Fetal Bovine Serum (Hyclone), Penicillin-Streptomycin and non-essential amino acids at 37° C. in a humidified 5% CO₂ atmosphere. On day 0, cells were harvested by trypsinization and 3×10⁶ cells (passage 13, 99% viability) in 0.1 mL of ice-cold Hank's balanced salt solution were implanted subcutaneously into the hindflank of 5-8 week old male nude mice. A transponder was implanted in each mouse for identification, and animals were monitored daily for clinical symptoms and survival. Body weights were recorded daily. Experiments were conducted with Compound A as a single agent as well as Compound A in combination with Taxol and Compound A in combination with Rapamycin. This model can be used to assess the desirability of treating with Compound A in combination with other anti-cancer agents.

U-87 MG human glioblastoma cells were cultured in vitro in DMEM (Mediatech) supplemented with 10% Fetal Bovine Serum (Hyclone), Penicillin-Streptomycin and non-essential amino acids at 37° C. in a humidified 5% CO₂ atmosphere. On day 0, cells were harvested by trypsinization and 2×10⁶ cells (passage 5, 96% viability) in 0.1 mL of ice-cold Hank's balanced salt solution were implanted intradermally into the hindflank of 5-8 week old female nude mice. A transponder was implanted in each mouse for identification, and animals were monitored daily for clinical symptoms and survival. Body weights were recorded daily. Experiments were conducted with Compound A as a single agent and the results are not included. This model can be used to assess the desirability of treating with Compound A in combination with other anti-cancer agents.

A549 human lung carcinoma cells were cultured in vitro in DMEM (Mediatech) supplemented with 10% Fetal Bovine Serum (Hyclone), Penicillin-Streptomycin and non-essential amino acids at 37° C. in a humidified 5% CO₂ atmosphere. On day 0, cells were harvested by trypsinization and 10×10⁶ cells (passage 12, 99% viability) in 0.1 mL of ice-cold Hank's balanced salt solution were implanted intradermally into the hindflank of 5-8 week old female nude mice. A transponder was implanted in each mouse for identification, and animals were monitored daily for clinical symptoms and survival. Body weights were recorded daily. Experiments were conducted with Compound A as a single agent as well as Compound A in combination with Compound B. This model can be used to assess the desirability of treating with Compound A in combination with other anti-cancer agents.

MDA-MB-468 human breast adenocarcinoma cells, passage number <6, were maintained and propagated in log-phase growth in Dulbecco's Modification of Eagles's Medium (DMEM; Mediatech) containing L-Glutamine supplemented with 10% Fetal Bovine Serum (Hyclone), Penicillin-Streptomycin and non-essential amino acids at 37° C. in a humidified, 5% CO₂ atmosphere. On day 0, cells were harvested by trypsinization, and 10×10⁶ cells (passage 10, 98% viability) in 50% cold Hanks balanced salt solution/50% Matrigel (100 μL total volume per mouse) were implanted subcutaneously into the mammary fat pads of female nude mice. Experiments were conducted with Compound A as a single agent as well as Compound A in combination with erlotinib. This model can be used to assess the desirability of treating with Compound A in combination with other anti-cancer agents.

Calu-6 human lung anaplastic carcinoma cells were cultured in vitro in DMEM (Mediatech) supplemented with 10% Fetal Bovine Serum (Hyclone), Penicillin-Streptomycin and non-essential amino acids at 37° C. in a humidified, 5% CO₂ atmosphere. On day 0, cells were harvested by trypsinization, and 5×10⁶ cells (passage #8, 96% viability) in 0.1 mL ice-cold Hank's balanced salt solution were implanted intradermally in the hind-flank of 5-8 week old female athymic nude mice. A transponder was implanted in each mouse for identification, and animals were monitored daily for clinical symptoms and survival. Body weights were recorded daily. Experiments were conducted with Compound A as a single agent as well as Compound A in combination with carboplatin. This model can be used to assess the desirability of treating with Compound A in combination with other anti-cancer agents.

MCF7 human mammary adenocarcinoma cells were cultured in vitro in DMEM (Cellgro) supplemented with 10% Fetal Bovine Serum (Cellgro), Penicillin-Streptomycin and non-essential amino acids at 37° C. in a humidified 5% CO₂ atmosphere. On day 0, cells were harvested by trypsinization, and 5×10⁶ cells (passage 10 and 95.4% viability for Study 1, passage 9 and 90% viability for Study 2) in 100 μL of a solution made of 50% cold Hanks balanced salt solution with 50% growth factor reduced matrigel (R&D Systems for Study 1 and Becton Dickinson for Study 2) implanted subcutaneously into the hindflank of female nude mice.

For subcutaneous or intradermal tumors, the mean tumor weight of each animal in the respective control and treatment groups was determined twice weekly during the study. Tumor weight (TW) was determined by measuring perpendicular diameters with a caliper, using the following formula:

tumor weight (mg)=[tumor volume=length (mm)×width² (mm²)]/2

These data were recorded and plotted on a tumor weight vs. days post-implantation line graph and presented graphically as an indication of tumor growth rates. Percent inhibition of tumor growth (TGI) is determined with the following formula:

$\left( {1 - \left( \frac{\left( {X_{f} - X_{0}} \right)}{\left( {Y_{f} - X_{0}} \right)} \right)} \right)*100$

-   -   where X₀=average TW of all tumors on group day     -   X_(f)=TW of treated group on Day f     -   Y_(f)=TW of vehicle control group on Day f         If tumors regress below their starting sizes, then the percent         tumor regression is determined with the following formula:

$\left( \frac{\left( {X_{0} - X_{f}} \right)}{X_{0}} \right)*100$

Tumor size is calculated individually for each tumor to obtain a mean±SEM value for each experimental group. Statistical significance is determined using the 2-tailed Student's t-test (significance defined as P<0.05).

Biological Examples 11-14

Compound A is a Compound of Formula I and is an inhibitor of class I PI3-kinases. Compound B is N-(3,4-dichloro-2-fluorophenyl)-7-({[(3aR,5r,6aS)-2-methyloctahydrocyclopenta-[c]pyrrol-5-yl]methyl}oxy)-6-(methyloxy)quinazolin-4-amine.

Prostate Cancer Xenograft Model—A Compound of Formula I in Combination with Taxol

Compound A was tested alone and in combination with taxol in a prostate carcinoma tumor model. PC-3 is a human prostate carcinoma cell line that harbors a homozygous deletion mutation in PTEN, which results in constitutive activation of the PI3K pathway. In single-dose pharmacodynamic experiments, oral administration of Compound A results in a dose-dependent decrease in the phosphorylation of AKT, p70S6K, and S6 in PC-3 tumors grown ectopically in mice. Repeat-dose administration of a Compound A also inhibits the growth of these tumors, but does not induce regressions.

Oral administration of Compound A at 100 mg/kg qd or 300 mg/kg biweekly (biw) resulted in substantial tumor growth inhibition in mice. See FIG. 1. Comparable tumor growth inhibition was achieved with 7.5 mg/kg taxol administered i.v. twice weekly. While tumor growth was inhibited substantially with Compound A alone, the combination of either dose of Compound A with taxol was superior to either agent alone and induced significant regression of the tumors. Body weight loss and dose skipping was minimal in all groups, and was not exacerbated in the combination group indicating that the combination was well tolerated. These results support the use of a Compound of Formula I in combination with taxol in tumors with constitutively activated PI3K signaling.

Prostate Cancer Xenograft Model—A Compound of Formula I in Combination with Rapamycin

Compound A was tested alone and in combination with rapamycin in a prostate carcinoma tumor model (PC-3 cell line). Oral administration of Compound A at 100 mg/kg qd resulted in substantial tumor growth inhibition. See FIG. 2. Comparable tumor growth inhibition was achieved with 5 mg/kg rapamycin administered i.p. daily. While tumor growth was inhibited substantially with Compound A alone, the combination of Compound A with rapamycin was superior to either agent alone and induced significant regression of the tumors. Body weight loss and dose skipping was minimal with each agent alone, but body weight loss was exacerbated in the combination group necessitating dose skipping. The fact that tumor regression was observed despite dose skipping suggests that using an intermittent dosing schedule would maintain efficacy and improve tolerability. These results support the use of a Compound of Formula I in combination with rapamycin in tumors with constitutively activated PI3K signaling.

Non-Small Cell Lung Cancer Xenograft Model—A Compound of Formula I in Combination with Carboplatin

Compound A was tested both as a single agent and in combination with carboplatin in a NSCLC tumor model.

Calu-6 is a human NSCLC cell line that harbors a heterozygous activating mutation in K-Ras (Q61K). Oral administration of a Compound A at 100 mg/kg qd or 300 mg/kg every fourth day (q4d) to mice bearing Calu-6 tumors resulted in substantial tumor growth inhibition. See FIG. 3. Both dose schedules resulted in similar inhibition of tumor growth. Significant tumor growth inhibition was also observed with 50 mg/kg carboplatin administered i.v. q4d, but was not as pronounced as with Compound A. While tumor growth was inhibited substantially with Compound A alone, the combination of the two agents was superior to either agent alone and resulted in almost complete inhibition of tumor growth. Body weight loss and dose skipping was minimal in all groups, and was not exacerbated in the combination group indicating that the combination was well tolerated. These results support the use of a Compound of Formula I both as a single agent and in combination with platins in tumors with activating mutations in K-Ras.

Non-Small Cell Lung Cancer Xenograft Model—A Compound of Formula I in Combination with Compound B

Compound A was tested both as a single agent and in combination with Compound B. The A549 human non-small cell lung carcinoma cell line harbors a homozygous stop mutation in the gene encoding LKB1, and an activating G125 mutation in K-Ras, promoting activation of both PI3K and mTOR. A549 cells also express wild-type EGFR.

As a single agent, Compound B, an inhibitor of EGFR, was orally administered once-daily at 30 mg/kg and Compound A was orally administered either at 30 mg/kg qd or 100 mg/kg q2d. Combination therapies consisted of Compound B with Compound A at 30 mg/kg or 100 mg/kg. Administration of each agent in the combination groups was separated by 6 h. Single agent administration of Compound B for 18 days caused a significant tumor growth inhibition of 80%. See FIG. 4 a. A significant tumor growth inhibition of 96% was observed with Compound A at 100 mg/kg q2d, whereas Compound A at 30 mg/kg qd lead to a lower but still significant TGI of 76%. The combination of Compound B 30 mg/kg qd with Compound A 30 mg/kg qd or with Compound A 100 mg/kg q2d resulted in significant efficacy associated with 15% and 39% regression, respectively, which was significantly higher than either of the single agent treatments alone.

As a single agent Compound B dosed at 30 mg/kg qd was generally well tolerated, with a body weight loss of 1.5-6.9% and no dose omission. Administration of Compound A dosed at 30 mg/kg qd was well tolerated with 4 doses skipped at the beginning of the study, which were not compound-related. Compound A dosed at 100 mg/kg q2d was also well tolerated with 1 dose skipped at the beginning of the study, which was not compound-related. The combination of Compound B at 30 mg/kg qd with Compound A at 30 mg/kg qd was fairly well tolerated with body weight loss of 1 to 8% and 2 doses skipped). However, the combination of Compound B at 30 mg/kg qd with Compound A at 100 mg/kg q2d was associated with body weight loss of 2 to 11% and 13 doses skipped within the first 10 days; however, body weights at the end of the study were not significantly different from the vehicle-treated control group. Single agent administration of Compound B and Compound A were well tolerated with minimal dose skipping. When administered in combination, minor body weight loss was observed that necessitated dose skipping primarily in the 100 mg/kg q2d group.

Breast Cancer Xenograft Model—A Compound of Formula I in Combination with Compound B

Compound A was tested both as a single agent and in combination with Compound B, an EGFR inhibitor, in a breast tumor model. The MCF7 human breast carcinoma cell line harbors a heterozygous, activating mutation in PI3K (PI3KCA/E545K) and expresses wild-type EGFR.

Compound B was administered orally once-daily (qd) at 30 mg/kg, and Compound A was administered once-daily at 30 mg/kg or once every other day (q2d) at 100 mg/kg. Combination therapies consisted of Compound B together with Compound A at 30 mg/kg qd or 100 mg/kg q2d. Single agent administration of Compound B at 30 mg/kg qd for 14 days caused a tumor growth inhibition of 38%-61%. See FIGS. 4 b-1 and 4 b-2. A significant tumor growth inhibition of 83%-91% was observed with Compound A at 100 mg/kg q2d, whereas Compound A at 30 mg/kg qd lead to a lower but still significant TGI of 57%. The combination of Compound B at 30 mg/kg qd with Compound A at 100 mg/kg q2d resulted in a significant efficacy associated with 16-22% regression, which was significantly higher than either of the single agent treatments alone. Combining Compound B at 30 mg/kg qd with Compound A at 30 mg/kg qd lead to a lower but still significant tumor growth inhibition of 66%, but did not add any benefit to the anti-tumor efficacy of the single treatments.

As a single agent Compound B dosed at 30 mg/kg qd was generally well tolerated, with a non significant final body weight loss of 4.5 to 6.1% and 7 to 13 dose omissions. Administration of Compound A at 30 mg/kg qd and 100 mg/kg q2d was well tolerated with minimal dose skipping and body weight loss. The combination of Compound B at 30 mg/kg qd with Compound A at 30 mg/kg qd lead to a body weight loss of 4 to 13% throughout the study and 14 doses skipped mostly within the first 9 days. The combination of Compound B at 30 mg/kg qd with Compound A at 100 mg/kg q2d was associated with a body weight loss of 3.7 to 13% throughout the study and 20 to 32 dose omissions.

Breast Cancer Xenograft Model—A Compound of Formula I in Combination with Erlotinib

Compound A was tested both as a single agent and in combination with erlotinib, in an erolitinib-resistant tumor model with elevated PI3K signaling.

MDA-MB-468 is a human breast carcinoma cell line that has an increase in the copy number of the EGFR gene and a homozygous deletion of PTEN. In vitro treatment of these cells with EGFR inhibitors such as erlotinib inhibits EGFR activity but fails to downregulate the PI3K pathway. Oral administration of erlotinib at 100 mg/kg qd to mice bearing MDA-MB-468 tumors resulted in significant but incomplete tumor growth inhibition. See FIG. 5. Oral administration of Compound A at 100 mg/kg qd resulted in a similar level of tumor growth inhibition. While tumor growth was inhibited substantially with Compound A alone, the combination of the two agents was superior to either agent alone and resulted in a regression of the tumors.

Mice administered Compound A at 100 mg/kg qd exhibited a modest (˜3%) loss in body weight comparable to vehicle controls. Mice administered erlotinib exhibited an apparent decrease in their rate of body weight gain relative to vehicle controls. Coadministration with erlotinib resulted in a substantial loss in body weight in mice treated with Compound A (19% body weight loss from start of dosing). Consistent with these data, only minimal dose-skipping was required when Compound A was administered as monotherapy (1-3 doses skipped), but substantial dose-skipping was required for Compound A when erlotinib was coadministered. The fact that tumor regression was observed despite dose skipping suggests that use of an intermittent dosing schedule could maintain efficacy and improve tolerability. These results support the use of a Compound of Formula I in combination with erlotinib in tumors expressing EGF receptors and harboring PTEN deletions.

The foregoing invention has been described in some detail by way of illustration and example, for purposes of clarity and understanding. It will be obvious to one of skill in the art that changes and modifications may be practiced within the scope of the appended claims. Therefore, it is to be understood that the above description is intended to be illustrative and not restrictive. The scope of the invention should, therefore, be determined not with reference to the above description, but should instead be determined with reference to the following appended claims, along with the full scope of equivalents to which such claims are entitled. All patents, patent applications and publications cited in this application are hereby incorporated by reference in their entirety for all purposes to the same extent as if each individual patent, patent application or publication were so individually denoted. 

1. A method of treating cancer which method comprises administering to a patient a therapeutically effective amount of a compound of Formula I:

or a single isomer thereof where the compound is optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof; or administering a pharmaceutical composition comprising a therapeutically effective amount of a Compound of Formula I and at least one of a pharmaceutically acceptable carrier, excipient, or diluent in combination with one or more treatments independently selected from surgery, one or more chemotherapeutic agents, one or more of the hormone therapies, one or more antibodies, one or more immunotherapies, radioactive iodine therapy, and radiation where the Compound of Formula I is that wherein: W¹, W², W³, and W⁴ are —C(R¹)═; or one or two of W¹, W², W³, and W⁴ are independently —N═ and the remaining are —C(R¹)═; and where each R¹ is independently hydrogen, alkyl, haloalkyl, nitro, alkoxy, haloalkoxy, halo, hydroxy, cyano, amino, alkylamino, or dialkylamino; R⁵¹ is hydrogen or alkyl; R⁵² is hydrogen or halo; R⁵⁰, R⁵³, and R⁵⁴ are independently hydrogen, alkyl, alkenyl, halo, haloalkyl, haloalkenyl, hydroxy, alkoxy, alkenyloxy, haloalkoxy, nitro, amino, alkylamino, dialkylamino, —N(R⁵⁵)C(O)—C₁-C₆-alkylene-N(R^(55a))R^(55b), alkylcarbonyl, alkenylcarbonyl, carboxy, alkoxycarbonyl, cyano, alkylthio, —S(O)₂NR⁵⁵R^(55a), or alkylcarbonylamino and where R⁵⁵ and R^(55b) are independently hydrogen, alkyl, or alkenyl and R^(55a) is hydrogen, alkyl, alkenyl, hydroxy, or alkoxy; or R⁵³ and R⁵⁴ together with the carbons to which they are attached form a 5- or 6-membered heteroaryl or 5- or 6-membered heterocycloalkyl; B is phenyl substituted with R^(3a) and optionally further substituted with one, two, or three R³; or B is heteroaryl optionally substituted with one, two, or three R³; R^(3a) is cyano; hydroxyamino; carboxy; alkoxycarbonyl; alkylamino; dialkylamino; alkylcarbonyl; haloalkoxy; alkylsulfonyl; aminoalkyloxy; alkylaminoalkyloxy; dialkylaminoalkyloxy; or a) —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)) where R⁷ is hydrogen, alkyl, or alkenyl and R^(7a) and R^(7b) are independently hydrogen, alkyl, alkenyl, hydroxyalkyl, haloalkyl, alkoxy, alkoxyalkyl, aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, heteroarylalkyl, aryl, arylalkyl, or arylalkyloxy and where the aryl, cycloalkyl, heterocycloalkyl and heteroaryl rings in R^(7a) and R^(7b) (either alone or as part of arylalkyl, cycloalkylalkyl, heterocycloalkylalkyl and heteroarylalkyl) are independently optionally substituted with 1, 2, or 3 groups independently selected from alkyl, amino, alkylamino, dialkylamino, hydroxy, halo, alkoxy, alkylthio, and oxo); b) —C(O)NR⁸R^(8a) where R⁸ is hydrogen, hydroxy, alkoxy, alkyl, alkenyl, haloalkyl, or haloalkoxy and R^(8a) is hydrogen, alkyl, alkenyl, hydroxyalkyl, cyanoalkyl, alkoxyalkyl, alkylthioalkyl, heterocycloalkyl, heterocycloalkylalkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, aryl, or arylalkyl and where the aryl, cycloalkyl, heteroaryl, and heterocycloalkyl rings in R^(8a) (either alone or as part of arylalkyl, cycloalkylalkyl, heterocycloalkylalkyl and heteroarylalkyl) are independently optionally substituted with 1, 2, or 3 groups independently selected from alkyl, alkenyl, alkoxy, halo, haloalkyl, haloalkoxy, hydroxy, hydroxyalkyl, oxo, amino, alkylamino, dialkylamino, alkylcarbonyl, aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, alkoxycarbonyl, and —C(O)H; c) —NR⁹C(O)R^(9a) where R⁹ is hydrogen, hydroxy, alkoxy, alkyl, alkenyl, haloalkyl, or haloalkoxy and R^(9a) is hydrogen, C₂-C₆-alkyl, alkenyl, hydroxyalkyl, alkoxyalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, heteroarylalkyl, aryl, or arylalkyl; where the aryl, cycloalkyl, heteroaryl, and heterocycloalkyl rings in R^(9a) (either alone or as part of arylalkyl, cycloalkylalkyl, heterocycloalkylalkyl and heteroarylalkyl) are independently optionally substituted with 1, 2, or 3 groups independently selected from alkyl, alkenyl, alkoxy, hydroxy, hydroxyalkyl, halo, haloalkyl, haloalkoxy, oxo, amino, alkylamino, dialkylamino, alkylcarbonyl, alkoxycarbonyl, —C(O)H, aryl (optionally substituted with one or two halo), arylalkyl, heteroaryl, heteroarylalkyl, heterocycloalkyl, heterocycloalkylalkyl, cyloalkyl, cyloalkylalkyl, and cycloalkylcarbonyl; d) —C(O)N(R¹⁰)—C₁-C₆-alkylene-N(R^(10a))R^(10b) where R^(10a) is hydrogen, hydroxy, alkoxy, alkyl, alkenyl, haloalkyl, aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, or hydroxyalkyl and R¹⁰ and R^(10b) are independently hydrogen, alkyl, alkenyl, haloalkyl, aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, or hydroxyalkyl; e) —NR¹¹C(O)NR^(11a)R^(11b) where R^(11a) is hydrogen, alkyl, alkenyl, hydroxy, or alkoxy and R¹¹ and R^(11b) are independently hydrogen, alkyl, alkenyl, aminoalkyl, alkylaminoalkyl, or dialkylaminoalkyl; f) —C(O)R¹² where R¹² is heterocycloalkyl optionally substituted with 1, 2, or 3 groups selected from alkyl, oxo, amino, alkylamino, and heterocycloalkylalkyl; g) —NR¹³C(O)OR^(13a) where R¹³ is hydrogen, alkyl, or alkenyl and R^(13a) is aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, aryl, or arylalkyl; h) —C(O)N(R¹⁴)N(R^(14a))(R^(14b)) where R¹⁴, R^(14a), and R^(14b) are independently hydrogen, alkyl, or alkenyl; i) —S(O)₂N(R¹⁵)—C₁-C₆-alkylene-N(R^(15a))R^(15b) where R¹⁵, R^(15a), and R^(15b) are independently hydrogen, alkyl, or alkenyl; j) —C(O)N(R¹⁶)—C₁-C₆-alkylene-C(O)OR^(16a) where R¹⁶ is hydrogen, alkyl, or alkenyl and R^(16a) is alkyl or alkenyl; k) heteroaryl optionally substituted with one or two aminoalkyl, alkylaminoalkyl, or dialkylaminoalkyl; l) —N(R¹⁷)—C(═N(R^(17b))(R^(17a)))(NR^(17c)R^(17d)), where R¹⁷, R^(17a), R^(17b), R^(17c), and R^(17d) are independently hydrogen, alkyl, or alkenyl; m) —N(R¹⁸)C(O)—C₁-C₆-alkylene-N(R^(18b))C(O)R^(18a) where R^(18a) is hydrogen, alkyl, alkenyl, or alkoxy and R¹⁸ and R^(18b) are independently hydrogen, alkyl, or alkenyl; n) —C(O)N(R¹⁹)—C₁-C₆-alkylene-C(O)R^(19a) where R¹⁹ is hydrogen, alkyl, or alkenyl and R^(19a) is amino, alkylamino, dialkylamino, or heterocycloalkyl; o) —N(R²⁰)C(O)—C₁-C₆-alkylene-C(O)R^(20a) where R²⁰ is hydrogen, alkyl, or alkenyl and R^(20a) is cycloalkyl or heterocycloalkyl; p) —NR²¹S(O)₂—C₁-C₆-alkylene-N(R^(21b))R^(21a) where R²¹ is hydrogen, alkyl, or alkenyl and R^(21a) and R^(21b) are independently hydrogen, alkyl, or alkenyl; q) —N(R²²)C(O)—C₁-C₆-alkylene-N(R^(22b))—N(R^(22c))(R^(22a)) where R²², R^(22a) and R^(22b) are independently hydrogen, alkyl, or alkenyl; r) —C₀-C₆-alkyl ene-N(R²³)—C₁₋C₆-alkylene-N(R^(23b))R^(23a) where R²³, R^(23a) and R^(23b) are independently hydrogen, alkyl, or alkenyl; or —NR²⁴C(O)—C₁₋C₆-alkylene-OR^(24a) where R²⁴ is hydrogen, alkyl, or alkenyl and R^(24a) is alkoxyalkyl or aryl optionally substituted with one or two halo or alkyl; and where each of the alkylene in R^(3a) is independently optionally further substituted with 1, 2, 3, 4, or 5 groups selected from halo, hydroxy, amino, alkylamino, and dialkylamino; and each R³ (when R³ is present) is independently alkyl; alkenyl; alkynyl; halo; hydroxy; oxo; alkoxy; cyano; hydroxyamino; carboxy; alkoxycarbonyl; amino; alkylamino; dialkylamino; alkylcarbonyl; haloalkoxy; alkylsulfonyl; aminoalkyloxy; alkylaminoalkyloxy; dialkylaminoalkyloxy; or a) —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)) where R⁷ is hydrogen, alkyl, or alkenyl and R^(7a) and R^(71i) are independently hydrogen, alkyl, alkenyl, hydroxyalkyl, haloalkyl, alkoxy, alkoxyalkyl, aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, heteroarylalkyl, aryl, arylalkyl, or arylalkyloxy and where the aryl, cycloalkyl, heterocycloalkyl and heteroaryl rings in R^(7a) and R^(7b) (either alone or as part of arylalkyl, cycloalkylalkyl, heterocycloalkylalkyl and heteroarylalkyl) are independently optionally substituted with 1, 2, or 3 groups independently selected from alkyl, amino, alkylamino, dialkylamino, hydroxy, halo, alkoxy, alkylthio, and oxo); b) —C(O)NR⁸R^(8a) where R⁸ is hydrogen, hydroxy, alkoxy, alkyl, alkenyl, haloalkyl, or haloalkoxy and R^(8a) is hydrogen, alkyl, alkenyl, hydroxyalkyl, cyanoalkyl, alkoxyalkyl, alkylthioalkyl, heterocycloalkyl, heterocycloalkylalkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, aryl, or arylalkyl and where the aryl, cycloalkyl, heteroaryl, and heterocycloalkyl rings in R^(8a) (either alone or as part of arylalkyl, cycloalkylalkyl, heterocycloalkylalkyl and heteroarylalkyl) are independently optionally substituted with 1, 2, or 3 groups independently selected from alkyl, alkenyl, alkoxy, halo, haloalkyl, haloalkoxy, hydroxy, hydroxyalkyl, oxo, amino, alkylamino, dialkylamino, alkylcarbonyl, aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, alkoxycarbonyl, and —C(O)H; c) —NR⁹C(O)R^(9a) where R⁹ is hydrogen, hydroxy, alkoxy, alkyl, alkenyl, haloalkyl, or haloalkoxy and R^(9a) is hydrogen, C₂-C₆-alkyl, alkenyl, hydroxyalkyl, alkoxyalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, heteroarylalkyl, aryl, or arylalkyl; where the aryl, cycloalkyl, heteroaryl, and heterocycloalkyl rings in R^(9a) (either alone or as part of arylalkyl, cycloalkylalkyl, heterocycloalkylalkyl and heteroarylalkyl) are independently optionally substituted with 1, 2, or 3 groups independently selected from alkyl, alkenyl, alkoxy, hydroxy, hydroxyalkyl, halo, haloalkyl, haloalkoxy, oxo, amino, alkylamino, dialkylamino, alkylcarbonyl, alkoxycarbonyl, —C(O)H, aryl (optionally substituted with one or two halo), arylalkyl, heteroaryl, heteroarylalkyl, heterocycloalkyl, heterocycloalkylalkyl, cyloalkyl, cyloalkylalkyl, and cycloalkylcarbonyl; d) —C(O)N(R¹⁰)—C₁-C₆-alkylene-N(R^(10a))R^(10b) where R^(10a) is hydrogen, hydroxy, alkoxy, alkyl, alkenyl, haloalkyl, or hydroxyalkyl and R¹⁰ and R^(10b) are independently hydrogen, alkyl, alkenyl, haloalkyl, or hydroxyalkyl; e) —NR¹¹C(O)NR^(11a)R^(11b) where R^(11a) is hydrogen, alkyl, alkenyl, hydroxy, or alkoxy and R¹¹ and R^(11b) are independently hydrogen, alkyl, alkenyl, aminoalkyl, alkylaminooalkyl, dialkylaminoalkyl; f) —C(O)R¹² where R¹² is heterocycloalkyl optionally substituted with 1, 2, or 3 groups selected from alkyl, oxo, amino, alkylamino, and heterocycloalkylalkyl; g) —NR¹³C(O)OR^(13a) where R¹³ is hydrogen, alkyl, or alkenyl and R^(13a) is aminoalkyl, alkylaminoalkyl, dialkylaminoalkyl, aryl, or arylalkyl); h) —C(O)N(R¹⁴)N(R^(14a))(R^(14b)) where R¹⁴, R^(14a), and R^(14b) are independently hydrogen, alkyl, or alkenyl; i) —S(O)₂N(R¹⁵)—C₁-C₆-alkylene-N(R^(15a))R^(15b) where R¹⁵, R^(15a), and R^(15b) are independently hydrogen, alkyl, or alkenyl; j) —C(O)N(R¹⁶)—C₁-C₆-alkylene-C(O)OR^(16a) where R¹⁶ is hydrogen, alkyl, or alkenyl and R^(16a) is alkyl or alkenyl; k) heteroaryl optionally substituted with one or two aminoalkyl, alkylaminoalkyl, or dialkylaminoalkyl; l) —N(R¹⁷)—C(═N(R^(17b))(R^(17a)))NR^(17c)R^(17d)) where R¹⁷, R^(17a), R^(17b), R^(17c), and R^(17d) are independently hydrogen, alkyl, or alkenyl; m) —N(R¹⁸)C(O)—C₁-C₆-alkylene-N(R^(18b))C(O)R^(18a) where R^(18a) is hydrogen, alkyl, alkenyl, or alkoxy and R¹⁸ and R^(18b) are independently hydrogen, alkyl, or alkenyl; n) —C(O)N(R¹⁹)—C₁-C₆-alkylene-C(O)R^(19a) where R¹⁹ is hydrogen, alkyl, or alkenyl and R^(19a) is amino, alkylamino, dialkylamino, or heterocycloalkyl; o) —N(R²⁰)C(O)—C₁-C₆-alkylene-C(O)R^(20a) where R²⁰ is hydrogen, alkyl, or alkenyl and R^(20a) is cycloalkyl or heterocycloalkyl; p) —NR²¹S(O)₂—C₁-C₆-alkylene-N(R^(21b))R^(21a) where R²¹ is hydrogen, alkyl, or alkenyl and R^(21a) and R^(21b) are independently hydrogen, alkyl, or alkenyl; q) —N(R²²)C(O)—C₁-C₆-alkylene-N(R^(22b))—N(R^(22c))(R^(22a)), where R²², R^(22a) and R^(22b) are independently hydrogen, alkyl, or alkenyl; r) —C₀₋C₆-alkylene-N(R²³)—C₁₋C₆-alkylene-N(R^(23b))R^(23a) where R²³, R^(23a) and R^(23b) are independently hydrogen, alkyl, or alkenyl; or s) —NR²⁴C(O)—C₁₋C₆-alkylene-OR^(24a) where R²⁴ is hydrogen, alkyl, or alkenyl and R^(24a) is alkoxyalkyl or aryl optionally substituted with one or two halo or alkyl; wherein each of the alkylene in R³ is independently optionally further substituted with 1, 2, 3, 4, or 5 groups selected from halo, hydroxy, amino, alkylamino, and dialkylamino; and provided that when R⁵⁰ and R⁵² are hydrogen, R⁵¹ is hydrogen or methyl, R⁵³ is hydrogen or methoxy, and R⁵⁴ is hydrogen or methoxy, then B is not 2,3-dihydro-1,4-benzodioxinyl, thien-2-yl, or thien-2-yl substituted with one R³ where R³ is halo.
 2. The method of claim 1 where the cancer is selected from breast cancer, colon cancer, rectal cancer, endometrial cancer, gastrointestinal carcinoid tumors, gastrointestinal stromal tumors, glioblastoma, hepatocellular carcinoma, small cell lung cancer, non-small cell lung cancer, melanoma, ovarian cancer, cervical cancer, pancreatic cancer, prostate carcinoma, acute myelogenous leukemia, chronic myelogenous leukemia, non-Hodgkin's lymphoma, and thyroid carcinoma. 3-6. (canceled)
 7. The method of claim 1 where the treatment is one chemotherapeutic agent and the chemotherapeutic agent is a platin.
 8. The method of claim 1 where the treatment is one chemotherapeutic agent and the chemotherapeutic agent is a taxane.
 9. The method of claim 1 where the treatment is one chemotherapeutic agent and the chemotherapeutic agent is rapamycin or a rapamycin analogue. 10-16. (canceled)
 17. The method of claim 1 where the Compound of Formula I is according to Formula I(a)

where W¹, W², W³, and W⁴ are —C(R¹)═; or one or two of W¹, W², W³, and W⁴ are independently —N═ and the remaining are —C(R¹)═; and where each R¹ is independently hydrogen, alkyl, haloalkyl, nitro, alkoxy, haloalkoxy, halo, hydroxy, cyano, amino, alkylamino, or dialkylamino; R⁵¹ is hydrogen or alkyl; R⁵² is hydrogen or halo; R⁵⁰, R⁵³, and R⁵⁴ are independently hydrogen, alkyl, alkenyl, halo, haloalkyl, haloalkenyl, hydroxy, alkoxy, alkenyloxy, haloalkoxy, nitro, amino, alkylamino, dialkylamino, —N(R⁵⁵)C(O)—C₁-C₆-alkylene-N(R^(55a))R^(55b), alkylcarbonyl, alkenylcarbonyl, carboxy, alkoxycarbonyl, cyano, alkylthio, —S(O)₂NR⁵⁵R^(55a), or alkylcarbonylamino and where R⁵⁵ and R^(55b) are independently hydrogen, alkyl, or alkenyl and R^(55a) is hydrogen, alkyl, alkenyl, hydroxy, or alkoxy; or R⁵³ and R⁵⁴ together with the carbons to which they are attached form a 5- or 6-membered heteroaryl or 5- or 6-membered heterocycloalkyl; R³ is not present or R³ is alkyl; and R^(3a) is —N(R⁷)C(O)—C₁-C₆-alkylene-N(R^(7a))(R^(7b)), —C(O)NR⁸R^(8a), —NR⁹C(O)R^(9a), or —C(O)N(R¹⁰)—C₁-C₆-alkylene-N(R^(10a))R^(10b); where each of the alkylene in R^(3a) is independently optionally further substituted with 1, 2, 3, 4, or 5 groups selected from halo, hydroxy, and amino; and where the compound is optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof.
 18. The method of claim 1 where the Compound of Formula I is selected from: N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)-6-oxo-1,6-dihydropyridine-3- sulfonamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-2,5-dimethylthiophene-3-sulfonamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-2,5-dichlorothiophene-3-sulfonamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-6-oxo-1,6-dihydropyridine-3-sulfonamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-6-chloropyridine-3-sulfonamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-3,5-dimethylisoxazole-4-sulfonamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-5-chloro-1,3-dimethyl-1H-pyrazole-4- sulfonamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-methyl-N- propylbenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- methylbutanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3- methylbutanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)pent-4-enamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)propanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)butanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2,2- dimethylpropanamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[2-(dimethylamino)- 1-methylethyl]benzamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-4-methylphenyl)- N²-methylglycinamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[2- (dimethylamino)ethyl]benzamide; 5-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[2- (dimethylamino)ethyl]-2-fluorobenzamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-pyrrolidin-3- ylbenzamide; 3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[2- (dimethylamino)ethyl]benzamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)glycinamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(2-pyrrolidin-1- ylethyl)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)glycinamide; N-(2-chloro-5-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²- methylglycinamide; 2-(dimethylamino)-N-(3-(N-(3-(3-(2-(dimethylamino)acetamido)-5-methoxyphenylamino)quinoxalin-2- yl)sulfamoyl)phenyl)acetamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-4-methylphenyl)-L- alaninamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-4-methylphenyl)- N²,N²-dimethylglycinamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-4-methylphenyl)-2- methylalaninamide; N-(2-aminoethyl)-3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-D-alaninamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[2- (dimethylamino)ethyl]-N-methylbenzamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- methylalaninamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-4-methylphenyl)-D- alaninamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²- methylglycinamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²- methylglycinamide; N-(3-{[(3-{[2-acetyl-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²,N²- dimethylglycinamide; N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-(formylamino)benzenesulfonamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-L- alaninamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²- ethylglycinamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-D- alaninamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(piperidin-2- ylmethyl)benzamide; N-(5-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-2- methylphenyl)glycinamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(1-methylazetidin-3- yl)benzamide; 2-azetidin-1-yl-N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)acetamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-L- prolinamide; N-(3-{[(3-{[2-bromo-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²- methylglycinamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(2-piperidin-1- ylethyl)benzamide; N²,N²-dimethyl-N-(3-{[(3-{[6-(methyloxy)quinolin-8-yl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)glycinamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[2- (diethylamino)ethyl]benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-L-alaninamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- methylalaninamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-4-methylphenyl)-N²,N²- dimethylglycinamide; 3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[2- (dimethylamino)ethyl]-N-methylbenzamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(1-methylpiperidin- 3-yl)benzamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-methyl- D-alaninamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-L-prolinamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-piperidin-3- ylbenzamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[(1-methylpiperidin- 2-yl)methyl]benzamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-4-cyanobenzenesulfonamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-[2- (dimethylamino)ethyl]-N²-methylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-D-serinamide; (2S)-2-amino-N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)butanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)azetidine-3- carboxamide; N-{2-[bis(2-hydroxyethyl)amino]ethyl}-3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}benzamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(1-ethylpiperidin-3- yl)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-[2- (dimethylamino)ethyl]-N²-methylglycinamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²,N²- dimethylglycinamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²,2- dimethylalaninamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-methyl-D- alaninamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}benzamide; 3-[(3-aminopyrrolidin-1-yl)carbonyl]-N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2- yl)benzenesulfonamide; N-(3-{[(3-{[2-bromo-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²,N²- dimethylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²- propylglycinamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-methyl- L-alaninamide; N-(5-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-2-methylphenyl)-beta- alaninamide; 5-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[2- (dimethylamino)ethyl]-2-(methyloxy)benzamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-(hydroxyamino)benzenesulfonamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)piperidine-3- carboxamide; N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-{[3-(methylamino)pyrrolidin-1- yl]carbonyl}benzenesulfonamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}benzoicacid; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(2-morpholin-4- ylethyl)benzamide; 3-{[3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[(1-ethylpyrrolidin- 2-yl)methyl]benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(4-methyl-1,4- diazepan-1-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²,N²- dimethylglycinamide; 3-[(4-amino-3-oxopyrazolidin-1-yl)carbonyl]-N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin- 2-yl)benzenesulfonamide; (2S)-2-amino-N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)butanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(2- hydroxypropyl)glycinamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(2- fluoroethyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-[(2- methylpropyl)oxy]glycinamide; 1-amino-N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)cyclopropanecarboxamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-(formylamino)benzenesulfonamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²- (cyclopropylmethyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-methyl-L- alaninamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-D-prolinamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-methylbenzamide; 3-[(3-aminoazetidin-1-yl)carbonyl]-N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2- yl)benzenesulfonamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[3- (dimethylamino)azetidin-1-yl]acetamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-D- prolinamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(pyridin-3- ylmethyl)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)piperidine-2- carboxamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)morpholine- 4-carboxamide; N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-cyanobenzenesulfonamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-pyrrolidin-1- ylacetamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)- N~6~,N~6~-dimethyl-L-lysinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-ethyl-N²- methylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(1H-imidazol- 4-yl)acetamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(pyridin-2- ylmethyl)benzamide; 1-amino-N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)cyclopentanecarboxamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(2- hydroxyethyl)benzamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(3-oxopyrazolidin-4- yl)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(2- methylpropyl)glycinamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-ethyl-N²- methylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1-(1H-imidazol- 4-ylmethyl)azetidine-3-carboxamide; N-(5-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-2-methylphenyl)- N²,N²-dimethylglycinamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[2-(1H-imidazol-4- yl)ethyl]benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1-ethylazetidine- 3-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-methyl-N²- (1-methylpyrrolidin-3-yl)glycinamide; N-(3-{[(2-{[3,5-bis(methyloxy)phenyl]amino}pyrido[2,3-b]pyrazin-3-yl)amino]sulfonyl}phenyl)-N²-[2- (dimethylamino)ethyl]-N²-methylglycinamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-(methylamino)benzenesulfonamide; N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-{[3-(dimethylamino)pyrrolidin-1- yl]carbonyl}benzenesulfonamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[(3S)-3- hydroxypyrrolidin-1-yl]acetamide; 1-amino-N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)cyclobutanecarboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²- butylglycinamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(3- piperidin-1-ylazetidin-1-yl)acetamide; 3-[(aminocarbonyl)amino]-N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2- yl)benzenesulfonamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1- hydroxycyclopropanecarboxamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(pyridin-4- ylmethyl)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(2,2- dimethylhydrazino)acetamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-[({[2- (dimethylamino)ethyl]amino}carbonyl)amino]benzenesulfonamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-methyl-N-(1- methylpyrrolidin-3-yl)benzamide; N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-{[3-(diethylamino)pyrrolidin-1- yl]carbonyl}benzenesulfonamide; N-(3-{[(3-{[3-fluoro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²- methylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- hydroxyacetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)pyridazine-4- carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1- methylpiperidine-4-carboxamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-1H-pyrrol-1- ylbenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(1- methylethyl)glycinamide; 1-amino-N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)cyclopentanecarboxamide; 1-amino-N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)cyclopropanecarboxamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(3-pyrrolidin-1- ylpropyl)benzamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(2-cyanoethyl)-N- methylbenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[3- (dimethylamino)pyrrolidin-1-yl]acetamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[2- (methyloxy)ethyl]benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-[2- (dimethylamino)ethyl]glycinamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-cyanobenzenesulfonamide; 2-(dimethylamino)ethyl(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)carbamate; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1- (cyclopropylmethyl)azetidine-3-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(1,1- dimethylethyl)glycinamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(2-cyanoethyl)-N- ethylbenzamide; 3-[(3-aminopiperidin-1-yl)carbonyl]-N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2- yl)benzenesulfonamide; N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-(1-{[2- (dimethylamino)ethyl]amino}ethyl)benzenesulfonamide; N²-methyl-N-(3-{[(3-{[3-(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1H-imidazole-2- carboxamide; 3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}benzoicacid; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[3- (dimethylamino)propyl]benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)isoxazole-5- carboxamide; N-(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(2,2,2- trifluoroethyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3-piperidin-1- ylpropanamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-morpholin-4- ylbenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3- oxocyclopentanecarboxamide; N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-[(2,2- dimethylhydrazino)carbonyl]benzenesulfonamide; 3-acetyl-N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)benzenesulfonamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[3-(1H-imidazol-1- yl)propyl]benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-6- hydroxypyridine-2-carboxamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[3- (diethylamino)propyl]benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(3-fluoro-4- hydroxyphenyl)glycinamide; N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)-N′-[2-(dimethylamino)ethyl]benzene-1,3- disulfonamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-4- (dimethylamino)butanamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(2- cyanoethyl)benzamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-4-[(difluoromethyl)oxy]benzenesulfonamide; methylN-[(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)carbonyl]-beta-alaninate; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[2- (methylthio)ethyl]benzamide; N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)-N′-[3-(dimethylamino)propyl]benzene- 1,3-disulfonamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[2- (ethylthio)ethyl]benzamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[2- (dimethylamino)ethyl]-N-ethylbenzamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[3-(2-oxopyrrolidin- 1-yl)propyl]benzamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(2-pyridin-4- ylethyl)benzamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[3- (ethyloxy)propyl]benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1-(furan-2- ylmethyl)azetidine-3-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)pyrimidine-5- carboxamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-(2H-tetrazol-5-yl)benzenesulfonamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1H-pyrrole-2- carboxamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(3-morpholin-4- ylpropyl)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-methyl-N²- (1-methylethyl)glycinamide; N-(3-{[(3-{[3-fluoro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²,N²- dimethylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1H-imidazole-4- carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²,N²- diethylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(3- methylisoxazol-5-yl)acetamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[3- (methyloxy)propyl]benzamide; N²,N²-dimethyl-N-(3-{[(3-{[2-methyl-5-(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-[(3- hydroxyphenyl)methyl]glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1-methyl-1H- pyrrole-2-carboxamide; 4-amino-N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)tetrahydro-2H-pyran-4-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[4- (methylamino)piperidin-1-yl]acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-piperidin-1- ylacetamide; N-(4-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²,N²- dimethylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1-methyl-L- prolinamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-(methylsulfonyl)benzenesulfonamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[3- (dimethylamino)propyl]-N-methylbenzamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[3- (propyloxy)propyl]benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)thiophene-3- carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1- (cyclopropylcarbonyl)azetidine-3-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(4- methylpiperazin-1-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1- (phenylmethyl)azetidine-3-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- chloropyridine-3-carboxamide; ethylN-[(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)carbonyl]-beta-alaninate; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-{3-[(1- methylethyl)oxy]propyl}benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-pyridin-4- ylacetamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(1,1-dimethyl-2- piperidin-1-ylethyl)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-methyl-N²- prop-2-en-1-ylglycinamide; N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-{5-[(dimethylamino)methyl]-1,3,4- oxadiazol-2-yl}benzenesulfonamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²- (phenylmethyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- (methyloxy)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1- propanoylazetidine-3-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)pyridine-3- carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-[2- (methyloxy)ethyl]glycinamide; 1-acetyl-N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)piperidine-4-carboxamide; N-{[(3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-4- methylphenyl)amino](dimethylamino)methylidene}-N-methylmethanaminium; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-4-[(trifluoromethyl)oxy]benzenesulfonamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(2- methylpyrrolidin-1-yl)acetamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-piperidin-1- ylbenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)furan-3- carboxamide; N²,N²-dimethyl-N-(3-{[(3-{[3-(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)glycinamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[1-methyl-2- (methyloxy)ethyl]benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-6- chloropyridine-3-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- chlorobenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-pyridin-2- ylacetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[3- (dimethylamino)azetidin-1-yl]acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[4- (dimethylamino)piperidin-1-yl]acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-pyridin-3- ylacetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(2- chlorophenyl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-[3- (dimethylamino)propyl]-N²-methylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-ethyl-N²-(2- hydroxyethyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[2- (phenylmethyl)pyrrolidin-1-yl]acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)furan-2- carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- chloropyridine-4-carboxamide; N²-acetyl-N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-4- chlorobenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-4- methylbenzamide; 1,1-dimethylethyl{2-[(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)amino]-2-oxoethyl}carbamate; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(1,1-dimethyl-2- morpholin-4-ylethyl)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1,3- benzodioxole-5-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-({[2- (methyloxy)phenyl]methyl}oxy)glycinamide; N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-({2-[(dimethylamino)methyl]piperidin- 1-yl}carbonyl)benzenesulfonamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)pyridine-4- carboxamide; N-(3-{[(3-{[4-fluoro-3-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²,N²- dimethylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[4-(3,4- dichlorophenyl)piperazin-1-yl]acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3-pyridin-3- ylpropanamide; N-[3-(butyloxy)propyl]-3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)tetrahydrofuran- 3-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-[(2- methylphenyl)methyl]glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(3- fluorophenyl)acetamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-[4-(diethylamino)-1- methylbutyl]benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(1-methyl-1- phenylethyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- methylcyclopropanecarboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-methyl-4- (methyloxy)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- methylpyridine-3-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-4- (methyloxy)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(4- ethylpiperazin-1-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)thiophene-2- carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3-fluoro-2- methylbenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- bromothiophene-3-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-4- fluorobenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(3- methylpiperidin-1-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- methylpropanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)pentanamide N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- (ethyloxy)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(2- fluorophenyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3- (dimethylamino)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(4- methylpiperidin-1-yl)acetamide; 3-{[(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}-N-(1,1-dimethyl-2-oxo- 2-piperidin-1-ylethyl)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(2- propylphenyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)pyrazine-2- carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3-fluoro-4- (methyloxy)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2,2- dimethylbutanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[(4- fluorophenyl)oxy]acetamide; 1-acetyl-N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)azetidine-3-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(4- methylphenyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²- phenylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(4-prop-2-en- 1-ylpiperazin-1-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- methylbenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3- (methyloxy)propanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3-methylfuran-2- carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²- [(phenylmethyl)oxy]glycinamide; N-{3-[({3-[(2-chloro-5-hydroxyphenyl)amino]quinoxalin-2-yl}amino)sulfonyl]phenyl}-N²,N²- dimethylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(3- chlorophenyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)cyclobutanecarboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[3- (methyloxy)phenyl]acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1- methylcyclopropanecarboxamide; N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-[(4-methylpiperazin-1- yl)carbonyl]benzenesulfonamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-6-{[2-(dimethylamino)ethyl]amino}pyridine- 3-sulfonamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3- fluorobenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-4- (dimethylamino)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3,4- dichlorobenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-{[2- (methylthio)phenyl]methyl}glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(2- fluorophenyl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-ethyl-N²-(1- methylethyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1,3-thiazole-4- carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-methyl-N²- (phenylmethyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(2- thienylmethyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(pyridin-2- ylmethyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3- (methyloxy)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-[(3-chloro-4- methylphenyl)methyl]glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- methylpentanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(4- chlorophenyl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3-fluoro-4- methylbenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[(2- methylphenyl)oxy]acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- cyclohexylacetamide; (1R,2R)—N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- phenylcyclopropanecarboxamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-(dimethylamino)benzenesulfonamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3- chlorobenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[2- (methyloxy)phenyl]acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3-[3- (methyloxy)phenyl]propanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(2-fluoro-4- methylphenyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-[(3- fluorophenyl)methyl]glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[4- (methyloxy)phenyl]acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- phenylacetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2,4- dichlorobenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3- oxocyclohexanecarboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(3- fluorophenyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(3- chlorophenyl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(2- phenylpropyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-[(2,4- dimethylphenyl)methyl]glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(2- methylpiperidin-1-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-[2- (methyloxy)phenyl]glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(3,4- dihydroisoquinolin-2(1H)-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(2- methylphenyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(4- oxopiperidin-1-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- fluorobenzamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-6-{[2-(dimethylamino)ethyl]oxy}pyridine-3- sulfonamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(1- phenylethyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-fluoro-6- (methyloxy)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-4-methyl-3- (methyloxy)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-[2-(1- methylethyl)phenyl]glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3-[2- (methyloxy)phenyl]propanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-4- methylpentanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(2- phenylmorpholin-4-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3-[4- (methyloxy)phenyl]propanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-cyclopentyl- N²-prop-2-en-1-ylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-methyl-N²- [2-(methyloxy)ethyl]glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-4-cyclopropyl-4- oxobutanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-[3-(1,1- dimethylethyl)phenyl]glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²- (cyclopropylmethyl)-N²-propylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(2- oxocyclopentyl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(4- chlorophenyl)glycinamide; 2-(1,4′-bipiperidin-1′-yl)-N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(4- cyclopentylpiperazin-1-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(2- methylphenyl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-[(5-fluoro-2- methylphenyl)methyl]glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3,3- dimethylbutanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(2- chlorophenyl)glycinamide N-(3-{[2-chloro-5-(methyloxy)phenyl]amino}quinoxalin-2-yl)-3-{[2-(piperidin-1-ylmethyl)piperidin-1- yl]carbonyl}benzenesulfonamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-5-fluoro-2- methylbenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-4-fluoro-3- methylbenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2,3- dichlorobenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- (phenyloxy)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-(2,3- dimethylphenyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-fluoro-5- methylbenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-{[(4- methylphenyl)methyl]oxy}glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[4-(1- methylethyl)piperazin-1-yl]acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(4- fluorophenyl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-4-methyl-2- (methyloxy)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(4- propylpiperidin-1-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[(3- methylphenyl)oxy]acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)tetrahydrofuran- 2-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-[3- (hydroxymethyl)piperidin-1-yl]acetamide; 1,1-dimethylethyl2-{[(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)amino]carbonyl}piperidine-1-carboxylate; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-methyl-N²- (pyridin-3-ylmethyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-ethyl-N²- phenylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-{[2- (methyloxy)ethyl]oxy}acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3- cyclopentylpropanamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2,5- dichlorobenzamide; 2-(4-acetylpiperazin-1-yl)-N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2- yl)amino]sulfonyl}phenyl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-5-fluoro-2- (methyloxy)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-cyclohexyl- N²-ethylglycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-5- methylisoxazole-3-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3- methylpyridine-2-carboxamide; N-(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)-6-(dimethylamino)pyridine-3-sulfonamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- (methyloxy)pyridine-3-carboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-3,5- dichlorobenzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(1,3- thiazolidin-3-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(4- formylpiperazin-1-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(2-pyridin-4- ylpiperidin-1-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2- (methyloxy)benzamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-N²-methyl-N²- (2-methylpropyl)glycinamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(4-formyl-1,4- diazepan-1-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-1- phenylcyclopropanecarboxamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(2,6- dimethylmorpholin-4-yl)acetamide; N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-(2- phenylpyrrolidin-1-yl)acetamide; and N-(3-{[(3-{[3,5-bis(methyloxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-morpholin-4- ylacetamide;

where the Compound is optionally as a pharmaceutically acceptable salt and additionally optionally as a hydrate and additionally optionally as a solvate thereof.
 19. The method of claim 1, 17, or 18 where the treatment is one antibody selected from an EGFR antibody and an ErbB2 antibody, or the treatment is one or two chemotherapeutic agents independently selected from rapamycin, a rapamycin analogue, an alkylating agent, a taxane, a platin, an EGFR inhibitor, and an ErbB2 inhibitor.
 20. The method of claim 19 where the treatment is one or two chemotherapeutic agents independently selected from rapamycin, paclitaxel, carboplatin, lapatinib, and erlotinib.
 21. (canceled)
 22. The method of claim 1, 17, or 18 where the treatment is one chemotherapeutic agent where the chemotherapeutic agent is erlotinib.
 23. The method of claim 1, 17, or 18 where the treatment is one chemotherapeutic agent where the chemotherapeutic agent is lapatinib.
 24. The method of claim 1, 17, or 18 where the treatment is one chemotherapeutic agent where the chemotherapeutic agent is carboplatin.
 25. The method of claim 1, 17, or 18 where the treatment is one chemotherapeutic agent where the chemotherapeutic agent is paclitaxel.
 26. The method of claim 1, 17, or 18 where the treatment is one chemotherapeutic agent where the chemotherapeutic agent is rapamycin.
 27. The method of claim 1, 17, or 18 where the treatment is one antibody selected from bevacizumab, trastuzumab, cetuximab, and panitumumab.
 28. (canceled)
 29. The method of claim 1, 17, or 18 where the treatment is one hormone therapy where the hormone therapy is an aromatase inhibitor.
 30. The method of claim 29 where the aromatase inhibitor is selected from letrozole, anastrozole, and exemestane.
 31. The method of claim 1 where the treatment is one antibody and the antibody is an ErbB2 antibody.
 32. The method of claim 17, 18, or 31 where the treatment is one antibody and the antibody is an ErbB2 antibody where the ErbB2 antibody is trastuzumab.
 33. The method of claim 1, 17, or 18 where the treatment is one or two agents independently selected from rapamycin, temozolomide, paclitaxel, docetaxel, carboplatin, trastuzumab, erlotinib, and lapatinib. 